Preparation of (E)- and (Z)-2-methyl-2-butenoic acids

ABSTRACT

A method has been developed to prepare (E)- and (Z)-2-methyl-2-butenoic acids (2M2BA) from a mixture of (E,Z)-2-methyl-2-butenenitriles (2M2BN) by the regioselective hydrolysis of (E)-2M2BN to (E)-2-methyl-2-butenoicacid (2M2BA) using enzyme catalysts having either a nitrilase activity or a combination of nitrile hydratase and amidase activities. The method provides high yields without significant conversion of (Z)-2M2BN to (Z)-2M2BA. The regioselective hydrolysis of (E)-2M2BN to (E)-2M2BA makes possible the facile separation of (E)-2M2BA from (Z)-2M2BN or (Z)-2-methyl-2-butenamide (2M2BAm), and the subsequent conversion of (Z)-2M2BN or (Z)-2M2BAm to (Z)-2M2BA.

FIELD OF THE INVENTION

[0001] The present invention relates to a biocatalytic, regioselective method for preparing (E)- and (Z)-2-methyl-2-butenoic acids (2M2BA) in high yields and two new microbial catalyst compositions useful in the method.

BACKGROUND OF THE INVENTION

[0002] (E)-2-methyl-2-buteneoic acid ((E)-2M2BA) (commonly known as tiglic acid) and (Z)-2-methyl-2-buteneoic acid ((Z)-2M2BA) (commonly known as angelic acid) are useful starting materials for preparing flavors and fragrances, and for preparing pharmaceutical intermediates.

[0003] (Z)-2M2BA has been prepared by the oxidation of the corresponding (Z)-alcohol with manganese dioxide, followed by the oxidation of the resulting aldehyde with sodium chlorite in the presence of hydrogen peroxide and sodium hydrogen phosphate (M. Zaidlewicz, Z. Walasek, PL 169502 B1 (1996)). R. E. Buckles and G. V. Mock reported the preparation of (E)-2M2BA in 53% yield by the action of 100% sulfuric acid on 2-hydroxy-2-methylbutyronitrile, followed by hydrolysis of the resulting (E)-2-methyl-2-butenamide (J. Org. Chem., 15:680-684 (1950)). The (E)-2M2BA produced by the Buckles-Mock process was further converted to (Z)-2M2BA in 33% yield by bromination of (E)-2M2BA to 2,3-dibromo-2-methylbutyric acid, debromination to (Z)-2-bromo-2-methylbutenoic acid using methanolic potassium hydroxide, followed by reduction of the bromo-acid using sodium amalgam.

[0004] (E)-2M2BA has been prepared in 89% yield by the carbonylation of 2-chloro-2-butene using catalytic quantities of cetyltrimethylammonium bromide and nickel cyanide (H. Alper et al., Tetrahedron Lett., 30:2615-2616 (1989)). Similarly, treatment of (E)- or (Z)-2-bromo-2-butene with carbon monoxide and octacarbonyldicolbalt in the presence of methyl iodide and calcium hydroxide in dioxane-water gave only (E)-2M2BA in 87-88% yield (M. Masahiro et al., J. Chem. Soc., Perkin Transactions 1 (1):73-76 (1989)). (E)-2M2BA has also been produced in 3% yield by UV irradiation of (Z)-2M2BA for 43 days, followed by separation of the (E)- and (Z)-isomers by a combination of fractional crystallizations and extractions (S. W. Pelletier and W. L. McLeish, J. Am. Chem. Soc., 74:6292-6293 (1952)).

[0005] Nitriles are readily converted to the corresponding carboxylic acids by a variety of chemical processes, but these processes typically require strongly acidic or basic reaction conditions, high reaction temperatures, and produce unwanted byproducts and/or large amounts of inorganic salts as unwanted waste. These chemical processes for nitrile hydrolysis are not known to result in the regioselective hydrolysis of mixtures of geometric isomers of nitrites. U.S. Pat. No. 5,041,646 describes a process where (E,Z)-2M2BN is reacted with sulfuric acid at elevated temperatures, followed by distillation of the product mixture to produce a mixture of 80.5% (Z)-2M2BA and 19.5% (E)-2M2BA; pure (Z)-2M2BA was prepared by fractional crystallization of the (E,Z)-2M2BA mixture. 2-Methyl-3-butenenitrile (2M3BN), a commercially-available by-product produced during the manufacture of adiponitrile by hydrocyanation of butadiene, is readily isomerized to a mixture of (E)-2M2BN and (Z)-2M2BN, but separating this mixture by distillation is difficult and expensive due to the similar boiling points and chemical properties of the geometric isomers.

[0006] The enzyme-catalyzed hydrolysis of nitrile-containing substrates to the corresponding carboxylic acids is often preferred to chemical methods because the reactions are often run at ambient temperature, do not require the use of strongly acidic or basic reaction conditions, and produce the desired product with high selectivity at high conversion.

[0007] A nitrilase enzyme directly converts a nitrile to the corresponding carboxylic acid ammonium salt in aqueous solution without the intermediate formation of an amide. Nitrilases have been identified in a variety of microorganisms. For example, Kobayashi et al. (Tetrahedron 46:5587-5590 (1990); J. Bacteriology, 172:4807-4815 (1990)) have described an aliphatic nitrilase isolated from Rhodococcus rhodochrous K22 that catalyzed the hydrolysis of aliphatic nitrites to their corresponding carboxylic acid ammonium salts. A nitrilase from Rhodococcus rhodochrous NCIMB 40757 or NCIMB 40833 has been used to convert acrylonitrile to ammonium acrylate (U.S. Pat. No. 5,998,180). A nitrilase from Comamonas testosteroni has been isolated that can convert a range of aliphatic α,ω-dinitriles to either the corresponding ω-cyanocarboxylic acid ammonium salt ordicarboxylic acid diammonium salt (CA 2,103,616; S. Levy-Schil et al., Gene, 161:15-20 (1995)). The regioselective hydrolysis of aliphatic α,ω-dinitriles to the corresponding ω-cyanocarboxylic acid ammonium salts by the nitrilase activity of Acidovorax facilis 72W has also been reported (Gavagan et al., J. Org. Chem., 63:4792-4801 (1998)). The nitrilase gene from Arthrobacter sp. NSSC104 has been cloned (WO 0314355), and a variety of bacterial nitrilases exhibiting stereoselectivity have been identified (WO 0300840).

[0008] A combination of two enzymes, nitrile hydratase and amidase, can also be used to convert aliphatic nitriles to the corresponding carboxylic acid ammonium salts in aqueous solution. Here the aliphatic nitrile is initially converted to an amide by the nitrile hydratase and then the amide is subsequently converted by the amidase to the corresponding carboxylic acid ammonium salt. Bacterial genera (including Rhodococcus, Pseudomonas, Alcaligenes, Arthrobacter, Bacillus, Bacteridium, Brevibacterium, Corynebacterium, and Micrococcus) are known to possess a broad spectrum of various nitrile hydratase and amidase activities. Cowan et al. (Extremophiles, 2:207-216 (1998)) and Martinkova and Kren (Biocatalysis and Biotransformation, 20:73-93 (2002)) have reviewed the nitrilase and nitrile hydratase/amidase enzyme systems of nitrile-degrading microorganisms.

[0009] Effenberger and Osswald (Tetrahedron, 12:2581-2587 (2001)) have reported the (E)-selective hydrolysis of (E,Z)-α,β-unsaturated nitriles by the recombinant nitrilase AtNIT1 from Arabidopsis thaliana, where the (E)-isomer of the (E,Z)-3-substituted-acrylonitrile mixtures was exclusively hydrolyzed in the presence of the corresponding (Z)-isomer; no 2,3-disubstituted acrylonitriles were examined as substrate for this nitrilase. When (E,Z)-3-heptenenitrile was used as substrate with this same nitrilase, enrichment of one isomer was not observed for either nitrile or acid. Almatawah et al. (Extremophiles, 3:283-291 (1999)) have reported that the nitrilase of Bacillus pallidus Dac521 showed no activity for hydrolysis of cis-2-pentenenitrile, but was capable of hydrolyzing acrylonitrile, methacrylonitrile, or crotononitrile; no 2,3-disubstituted acrylonitriles were examined as substrate for this nitrilase. Zhao and Wang (Chinese J. Chem., 20:1291-1299 (2002)) demonstrated that the combined nitrile hydratase and amidase activities of Rhodococcus sp. AJ270 could be used for the enantioselective biotransformation of racemic p-substituted-α-methylenepropionitriles. Where the amidase was shown by Zhao and Wang supra to discriminate between the two amide hydration products produced by the nitrile hydratase, no 2,3-disubstituted acrylonitriles were examined as substrate for this combination of nitrile hydratase/amidase enzymes.

[0010] The problem to be solved, therefore, is the lack of a process for the facile preparation of (E)- and (Z)-2M2BA from a mixture of (E,Z)-2M2BN using an enzyme catalyst having either nitrilase activity or a combination of nitrile hydratase and amidase activities, where the enzyme catalyst is regioselective for the hydrolysis or hydration of one of the two geometric isomers of (E,Z)-2M2BN.

SUMMARY OF THE INVENTION

[0011] A process is disclosed for preparing (E)- and (Z)-2-methyl-2-butenoic acids (2M2BA) in high yield and purity from a mixture of (E,Z)-2-methyl-2-butenenitriles (2M2BN) by the regioselective hydrolysis of (E)-2M2BN to (E)-2-methyl-2-butenoic acid (2M2BA), without significant conversion of (Z)-2M2BN to (Z)-2M2BA. The invention has the steps of (a) contacting (E,Z)-2M2BN in an aqueous reaction mixture with an enzyme catalyst expressing a regioselective nitrilase activity; (b) separating the (E)-2M2BA produced in step (a) from unreacted (Z)-2M2BN, and (c) converting (Z)-2M2BN to (Z)-2M2BA. More particularly, (E)-2M2BN is converted to the corresponding carboxylic acid (as the ammonium salt) with high regioselectivity at 100% conversion, using a regioselective nitrilase as catalyst. The regioselective hydrolysis of (E)-2M2BN to (E)-2M2BA (as the ammonium salt) makes possible the facile separation of (E)-2M2BA from (Z)-2M2BN, and for the subsequent conversion of (Z)-2M2BN to (Z)-2M2BA in high yield and purity.

[0012] Microorganisms characterized by a nitrilase activity and useful in the process are Acidovorax facilis 72-PF-15 (ATCC 55747) and Acidovorax facilis 72-PF-17 (ATCC 55745). Additionally, transformed microbial cells containing A. facilis 72W nitrilase activity are included in this invention. Escherichia coli SS1001 (ATCC PTA-1177) and Escherichia coli SW91 (ATCC PTA-1175) are examples of such a transformed microbial cell catalyst.

[0013] A further embodiment of the invention is the use of the A. facilis 72W (ATCC 55746) strain that expresses (1) regioselective and chemoselective nitrilase activity and (2) a nitrile hydratase and amidase activity, as an enzyme catalyst for regioselective hydrolysis of (E)-2M2BN to (E)-2M2BA. Prior to use as catalyst, whole A. facilis 72W (ATCC 55746) microbial cells are heated to a temperature of about 35° C. to 70° C. for between 10 and 120 minutes, whereby the nitrile hydratase and amidase activity is destroyed and the regioselective nitrilase activity is preserved. Where the transformed whole microbial cell expresses regioselective and chemoselective nitrilase activity and lacks nitrile hydratase and amidase activities, no heat-treatment step is needed. Escherichia coli SS1001 (ATCC PTA-1177) and Escherichia coli SW91 (ATCC PTA-1175) are examples of a transformed microbial cell catalyst that lack nitrile hydratase and amidase activities.

[0014] A further embodiment of the invention uses a catalyst having a combination of a regioselective nitrile hydratase and amidase activities. The invention has the steps of (a) contacting (E,Z)-2M2BN in an aqueous reaction mixture with an enzyme catalyst expressing a combination of regioselective nitrile hydratase and amidase activities; (b) separating the (E)-2M2BA produced in step (a) from unreacted (Z)-2M2BN and/or (Z)-2M2BAm, and (c) conversion of (Z)-2M2BN and/or (Z)-2M2BAm to (Z)-2M2BA. More particularly, (E)-2M2BN is converted to the corresponding carboxylic acid (as the ammonium salt) with high regioselectivity at 100% conversion, by a combination of regioselective nitrile hydratase and amidase activities derived from the group of microbial catalysts consisting of Comamonas testosteroni 5-MGAM-4D, Comamonas testosteroni S2B-1 (ATCC PTA-5135), and Comamonas testosteroni S5C (ATCC PTA-5134). The regioselective hydrolysis of (E)-2M2BN to (E)-2M2BA makes possible the facile separation of (E)-2M2BA from unreacted (Z)-2M2BN and/or (Z)-2M2BAm), and for the subsequent conversion of (Z)-2M2BN and/or (Z)-2M2BAm to (Z)-2M2BA.

[0015] Further embodiments of the invention use an enzyme catalyst in the form of intact microbial cells, permeabilized microbial cells, one or more cell components of a microbial cell extract, and partially-purified enzyme(s), or purified enzyme(s). These different forms of enzyme catalyst can be immobilized on or in a soluble or insoluble support using techniques well-known to those skilled in the art.

SEQUENCE DESCRIPTIONS

[0016] The invention can be more fully understood from the following detailed description, biological deposits, and the accompanying sequence descriptions, which form a part of this application.

[0017] The following sequences comply with 37 C.F.R. 1.821-1.825 (“Requirements for Patent Applications Containing Nucleotide Sequences and/or Amino Acid Sequence Disclosures—the Sequence Rules”) and are consistent with World Intellectual Property Organization (WIPO) Standard ST.25 (1998) and the sequence listing requirements of the EPO and PCT (Rules 5.2 and 49.5(a-bis), and Section 208 and Annex C of the Administrative Instructions). The symbols and format used for nucleotide and amino acid sequence data comply with the rules set forth in 37 C.F.R. §1.822.

[0018] SEQ ID NO:1 is the nucleotide sequence encoding a nitrilase isolated from Acidovorax facilis 72W (ATCC 55746).

[0019] SEQ ID NO:2 is the deduced amino acid sequence of a nitrilase isolated from Acidovorax facilis 72W.

[0020] SEQ ID NO:3 is the nucleotide sequence encoding a nitrilase expressed in Escherichia coli SS1001 (ATCC PTA-1177).

[0021] SEQ ID NO:4 is the deduced amino acid sequence of a nitrilase expressed in Escherichia coli SS1001.

[0022] SEQ ID NO:5 is the nucleotide sequence encoding the a-subunit of a nitrilase hydratase isolated from Comamonas testosteroni 5-MGAM-4D (ATCC 55744).

[0023] SEQ ID NO:6 is the deduced amino acid sequence of the nitrile hydratase α-subunit isolated from Comamonas testosteroni 5-MGAM-4D.

[0024] SEQ ID NO:7 is the nucleotide sequence encoding the p-subunit of a nitrilase hydratase isolated from Comamonas testosteroni 5-MGAM-4D.

[0025] SEQ ID NO:8 is the deduced amino acid sequence of the nitrile hydratase β-subunit isolated from Comamonas testosteroni 5-MGAM-4D.

[0026] SEQ ID NO:9 is the nucleotide sequence encoding an amidase isolated from Comamonas testosteroni 5-MGAM-4D.

[0027] SEQ ID NO:10 is the deduced amino acid sequence of the amidase isolated from Comamonas testosteroni 5-MGAM-4D.

BRIEF DESCRIPTION OF THE BIOLOGICAL DEPOSITS

[0028] Applicants have made the following biological deposits under the terms of the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure: Depositor Identification Int'l. Depository Reference Designation Date of Deposit Acidovorax facilis 72-PF-17 ATCC 55745  8 Mar. 1996 Acidovorax facilis 72W ATCC 55746  8 Mar. 1996 Acidovorax facilis 72-PF-15 ATCC 55747  8 Mar. 1996 Escherichia coli SS1001 ATCC PTA-1177 11 Jan. 2000 Escherichia coli SW91 ATCC PTA-1175 11 Jan. 2000 Comamonas testosteroni 5- ATCC 55744  8 Mar. 1996 MGAM-4D Comamonas testosteroni S2B-1 ATCC PTA-5135 11 Apr. 2003 Comamonas testosteroni S5C ATCC PTA-5134 11 Apr. 2003

[0029] As used herein, “ATCC” refers to the American Type Culture Collection International Depository Authority located at ATCC, 10801 University Blvd., Manassas, Va. 20110-2209, USA. The “International Depository Designation” is the accession number to the culture on deposit with ATCC.

[0030] The listed deposits will be maintained in the indicated international depository for at least thirty (30) years and will be made available to the public upon the grant of a patent disclosing it. The availability of a deposit does not constitute a license to practice the subject invention in derogation of patent rights granted by government action.

DETAILED DESCRIPTION OF THE INVENTION

[0031] Applicants have solved the stated problem by providing a process to prepare (E)- and (Z)-2-methyl-2-butenoic acids (2M2BA) in high yield and at high concentration in the reaction mixture starting from a mixture of (E,Z)-2-methyl-2-butenenitriles (2M2BN) and using a catalyst having either a nitrilase activity or a combination of nitrile hydratase and amidase activities. Applicants have isolated and characterized two new microbial catalysts, C. testosteroni S2B-1 (ATCC PTA-5135) and C. testosteroni S5C. (ATCC PTA-5134), which have a combination of regioselective nitrile hydratase and amidase activities useful for converting the (E)-2M2BN component of (E,Z)-2M2BN to (E)-2M2BA, without concomitant hydrolysis of (Z)-2M2BN to (Z)-2M2BA.

[0032] The method employs an enzyme catalyst that regioselectively hydrolyzes (E)-2M2BN to (E)-2-methyl-2-butenoic acid (2M2BA). The method provides high yields without significant conversion of (Z)-2M2BN to (Z)-2M2BA. The regioselective hydrolysis of (E)-2M2BN to (E)-2M2BA makes possible the facile separation of (E)-2M2BA (as the ammonium salt) from (Z)-2M2BN or (Z)-2-methyl-2-butenamide (2M2BAm), and for the subsequent conversion of (Z)-2M2BN or (Z)-2M2BAm to (Z)-2M2BA.

[0033] (E)- and (Z)-2M2BA are useful for preparing flavor and fragrance ingredients, as well as in for preparing pharmaceutical intermediates. The process has the added industrial advantages of low temperature and energy requirements and low waste or byproduct production relative to previously known chemical methods.

[0034] Microbial catalysts can hydrolyze a nitrile directly to the corresponding carboxylic acids using 1) a nitrilase (EC 3.5.5.7) enzyme without intermediate production of the corresponding amide (Equation 1), or 2) a combination of nitrile hydratase (EC 4.2.1.84) and amidase (EC 3.5.1.4) enzymes, in which case a nitrile hydratase (NHase) initially converts a nitrile to an amide, and then the amide is subsequently converted by the amidase to the corresponding carboxylic acid

[0035] In the present invention, microbial catalysts having nitrilase activity, or a combination of nitrile hydratase and amidase activities, have been identified which can convert the (E)-2M2BN component of a mixture of (E,Z)-2M2BN with high regiospecificity to the corresponding carboxylic acid at high concentration and at complete conversion of the nitrile. The process gives no significant conversion of (Z)-2M2BN to (Z)-2M2BA. The identified catalysts of the present invention eliminate the need for close monitoring over the course of the reaction to maintain a low concentration of nitrile, and do not require the reaction be run at a low temperature (5-10° C.) to maintain the stability of the enzyme catalyst. Instead, the process uses either a thermally-stable nitrilase or a combination of nitrile hydratase and amidase enzymes as catalysts for the desired conversions.

[0036] U.S. Pat. No. 5,858,736 describes using the nitrilase activity of a microbe, Acidovorax facilis 72W (ATCC 55746), as a catalyst for the hydrolysis of aliphatic α,ω-dinitriles to the corresponding ω-cyanocarboxylic acids and ammonia in an aqueous reaction mixture. The nitrilase catalyzed the hydrolysis of an α-alkyl-α,ω-dinitrile to the ω-cyanocarboxylic acid resulting from hydrolysis of the ω-cyano group with at least 98% regioselectivity at 100% conversion. U.S. Pat. No. 5,814,508 describes a process whereby heating a suspension of Acidovorax facilis 72W (ATCC 55746) in a suitable buffer at 50° C. for a short period of time deactivates an undesirable nitrile hydratase and amidase activity of the whole-cell catalyst, without producing a significant decrease in the desired nitrilase activity.

[0037] The complete regioselectivity of the nitrilase catalysts of the present invention for hydrolysis of only (E)-2-methyl-2-butenenitrile to the corresponding carboxylic acid, with no detectable hydrolysis of (Z)-2-methyl-2-butenenitrile under the same reaction conditions, was unexpected and could not have been predicted. U.S. Pat. No. 5,858,736 describes the use of the nitrilase catalysts of the present invention for the hydrolysis of 2-methylglutaronitrile and 2-methyleneglutaronitrile to the corresponding ω-cyanocarboxylic acids; for the hydrolysis of 2-methylglutaronitrile, no 2-methyl-4-cyanobutanoic acid was produced, and 2-methylglutaric acid was produced at <2% total yield at complete conversion of 2-methylglutaronitrile, whereas for hydrolysis of 2-methylenegluraronitrile, 4-cyano-4-pentenoic acid was the only hydrolysis product, and there was no hydrolysis of the cyano group vicinal to the α-methylene substituent.

[0038] In contrast, the accompanying examples demonstrate that the nitrilase catalysts described in U.S. Pat. No. 5,858,736 are capable of catalyzing the complete conversion of 2-methyl-3-butenenitrile, (cis)-2-pentenenitrile, and (trans)-2-pentenenitrile to the corresponding carboxylic acids. Neither the presence or absence of a methyl or methylene substituent at the α-position relative to a cyano group, nor the presence or absence of α,β-unsaturation relative to the position of a cyano group, could be used to predict if an α-alkyl substituted nitrile is a substrate for the nitrilase catalysts of the present invention. Similarly, it could not have been predicted whether or not the nitrile hydratase and amidase catalysts of the present invention would exhibit regioselectivity towards hydrolysis of geometric isomers of 2,3-disubstituted acrylonitriles such as (E)- and (Z)-2-methyl-2-butenenitrile.

[0039] It was also not previously known nor predicted before Applicants' invention that the regioselective nitrilase biocatalysts derived from Acidovorax facilis 72W would be stable to the high concentrations of (E,Z)-α,β-unsaturated nitrile and (E)-α,β-unsaturated carboxylic acid present over the course of a single reaction, or over the course of a series of reactions when the catalyst was recycled to produce (E)-2M2BA at high concentration. In particular, the nitrilase enzyme of the present invention relies on the sulfhydryl group of a cysteine in the active site of the enzyme for its catalytic activity (WO 0175077 A2), and α,β-unsaturated nitriles, amides and carboxylic acids are known to be highly reactive towards sulfhydryl groups, where a sulfhydryl group may react at the i-position of these compounds and thereby irreversibly inactivate the enzyme.

[0040] U.S. Pat. No. 5,858,736 also describes the use of a combination of a regioselective nitrile hydratase and amidase activities of C. testosteroni 5-MGAM-4D (ATCC 55744), as catalyst for the hydrolysis of aliphatic α,ω-dinitriles to the corresponding o)-cyanocarboxylic acids in an aqueous reaction mixture. This microbe exhibits both non-regioselective and regioselective nitrile hydratase activities, but heating a suspension of C. testosteroni 5-MGAM-4D in a suitable buffer at 50° C. for a short period of time deactivates the undesirable non-regioselective nitrile hydratase of the microbial cell catalyst, without producing a significant decrease in the desired regioselective nitrile hydratase and amidase activities. In the present application, no heat-treatment of C. testosteroni 5-MGAM-4D is required for regioselective hydrolysis of (E)-2M2BN to (E)-2M2BA, where there is no concomitant hydrolysis of (Z)-2M2BN to (Z)-2M2BA.

[0041] Microbial Catalysts

[0042] Applicants have isolated and characterized two new microbial catalysts, C. testosteroni S2B-1 (ATCC PTA-5135) and C. testosteroni S5C (ATCC PTA-5134), which have a combination of regioselective nitrile hydratase and amidase activities useful for converting the (E)-2M2BN component of (E,Z)-2M2BN to (E)-2M2BA, without concomitant hydrolysis of (Z)-2M2BN to (Z)-2M2BA.

[0043] In the present invention, the C. testosteroni catalysts utilize two enzyme activities to convert (E)-2M2BN to (E)-2M2BA. It was not previously known (and could not have been predicted) that both the regioselective nitrile hydratase and amidase enzymes would be stable to the high concentrations of α,β-unsaturated nitriles, amides, and carboxylic acids present over the course of a single reaction or over the course of a series of reactions when the catalyst was recycled to produce (E)-2M2BA at high concentration. All known amidase enzymes, including those of the present invention, rely on the sulfhydryl group of a cysteine in the active site of the enzyme for their catalytic activity, and α,β-unsaturated nitriles, amides, and carboxylic acids are known to be highly reactive towards sulfhydryl groups, where a sulfhydryl group may react at the 5-position of the compounds and thereby irreversibly inactivate the enzyme.

[0044] Definitions:

[0045] In this disclosure, a number of terms and abbreviations are used. The following definitions apply unless specifically stated otherwise.

[0046] “Catalyst”, “enzyme catalyst”, or “microbial cell catalyst” refer to a catalyst expressing a nitrilase activity or a combination of nitrile hydratase and amidase activities. The catalyst may be in the form of an intact microbial cell, permeabilized microbial cell(s), one or more cell components of a microbial cell extract, partially-purified enzyme(s), or purified enzyme(s).

[0047] The term “thermally-stable” characterizes an enzyme that retains activity despite exposure to a given temperature.

[0048] The terms “Comamonas testosteroni” and “C. testosteroni” are used interchangeably.

[0049] The terms “Acidovorax facilis” and “A. facilis” are used interchangeably.

[0050] The terms “Escherichia coli” and “E. coli” are used interchangeably.

[0051] The term “(E)-2-methyl-2-butenenitrile” is synonymous with (E)-2-methylcrotononitrile, tiglonitrile, trans-2-methyl-2-butenenitrile, and all other synonyms of CAS Registry Number 30574-97-1.

[0052] The term “(Z)-2-methyl-2-butenenitrile” is synonymous with (Z)-2-methylcrotononitrile, angelonitrile, cis-2-methyl-2-butenenitrile, and all other synonyms of CAS Registry Number 20068-02-4.

[0053] The term “2-methyl-3-butenenitrile” is synonymous with 3-cyanobut-1-ene, and all other synonyms of CAS Registry Number 16529-56-9.

[0054] The term “(E)-2-methyl-2-butenoic acid” is synonymous with (E)-2-methylcrotonic acid, tiglic acid, (E)-α-methylcrotonic acid, (E)-2,3-dimethylacrylic acid, (E)-2-methylcrotonic acid, cevadic acid, tiglinic acid, trans-α,β-dimethylacrylic acid, trans-2,3-dimethylacrylic acid, trans-2-methyl-2-butenoic acid, trans-2-methylcrotonic acid, and all other synonyms of CAS Registry Number 80-59-1.

[0055] The term “(Z)-2-methyl-2-butenoic acid” is synonymous with (Z)-2-methylcrotonic acid, angelic acid, (Z)-α-methylcrotonic acid, (Z)-2,3-dimethylacrylic acid, (Z)-2-methylcrotonic acid, cis-α,β-dimethylacrylic acid, cis-2,3-dimethylacrylic acid, cis-2-methyl-2-butenoic acid, cis-2-methylcrotonic acid, and all other synonyms of CAS Registry Number 565-63-9.

[0056] The term “(E)-2-methyl-2-butenamide” is synonymous with (E)-2-methylcrotonamide, tiglic acid amide, tiglamide, and all other synonyms of CAS Registry Number 6028-38-2.

[0057] The term “(Z)-2-methyl-2-butenamide” is synonymous with (Z)-2-methylcrotonamide, angelic acid amide, angelamide, and all other synonyms of CAS Registry Number 5953-75-3.

[0058] The term “suitable aqueous reaction mixture” refers to the materials and water in which the nitrile substrate and enzyme catalyst come into contact. Components of suitable aqueous reaction mixtures are referred to herein and those skilled in the art appreciate the range of component variations suitable for this process.

[0059] The abbreviations in the specification correspond to units of measure, techniques, properties, or compounds as follows: “sec” means second(s), “min” means minute(s), “h” means hour(s), “d” means day(s), “mL” means milliliters, “L” means liters, “mM” means millimolar, “M” means molar, “mmol” means millimole(s), and “wt” means weight. “HPLC” means high performance liquid chromatography, “ca” means approximately, “O.D.” means optical density at the designated wavelength, “IU” means International Units.

[0060] Methods and Materials:

[0061] Growth of Acidovorax facilis Strain 72W (ATCC 55746)

[0062] One frozen seed lot vial of Acidovorax facilis strain 72W (ATCC 55746) was thawed and the 1 mL contents placed in 500 mL of sterile Inoculum Medium listed below. The inoculurn was grown at 30° C. with shaking at 250 rpm in a two L flask for 24-301 h. Inoculum Medium Component: Final Concentration: Potassium phosphate, monobasic 1.5 g/L Potassium phosphate, dibasic 3.4 g/L Ammonium sulfate 1.5 g/L Trisodium citrate, dihydrate 1 g/L Magnesium sulfate, heptahydrate 0.4 g/L Trace metal solution (below) 1 mL/L Amberex 695 (Universal Foods) 1 g/L Glycerol (sterilized separately) 8 g/L Trace Metal Solution Component: Stock Concentration: Hydrochloric Acid 10 mL/L Calcium chloride, dihydrate 11.4 g/L Manganese Sulfate, monohydrate 1.23 g/L Copper sulfate, pentahydrate 0.63 g/L Cobalt chloride, hexahydrate 0.16 g/L Boric Acid 0.91 g/L Zinc sulfate, heptahydrate 1.77 g/L Sodium molybdate, dihydrate 0.05 g/L Vanadyl sulfate, dihydrate 0.08 g/L Nickel nitrate, hexahydrate 0.04 g/L Sodium selenite 0.04 g/L Ferrous sulfate, heptahydrate 6.00 g/L

[0063] The inoculum from the shake flask was transferred aseptically to a pre-sterilized Braun Biostat C fermentor containing Fermentor Medium listed below. Growth occurred under the following conditions: 32° C., pH 6.8-7.0, dissolved oxygen at 25% of saturation. At inoculation the fermentor contained 8.5 L of Fermentor Medium plus 218 g of Nutrient Feed solution, giving a starting concentration of approximately 7 g/L glycerol. The Nutrient Feed solution includes the following components that were sterilized separately and combined after cooling: potassium phosphate, monobasic, 19.6 g in 0.25 L deionized water; magnesium sulfate, heptahydrate, 3.3 g, plus sulfuric acid, 4 mL, in 0.15 L deionized water; Trace Metal solution, 67 mL, plus 400 g glycerol in 0.80 L deionized water. At 18 h post inoculation, feeding of Nutrient Feed solution began. Initially, the Nutrient Feed solution was added at a rate of 0.4 g feed/minute (0.15 g glycerol/min). The culture OD 550 was approximately 8-9. At 26 h, the feed rate was increased to 0.9 g feed/minute (0.3 g glycerol/min). The OD 550 was approximately 16-18. A final increase in feed rate to 1.8 g feed/minute (0.6 g glycerol/min) was made at 34 h. This rate was maintained to the end of run (about 42 h). The final OD 550 was approximately 65-75. Fermentor Medium Component: Final Concentration: Potassium phosphate, monobasic 0.39 g/L Potassium phosphate, dibasic 0.39 g/L Difco yeast extract  5.0 g/L

[0064] Cells, as wet cell paste, were recovered by centrifugation and stored frozen until use. Dry cell weight of wet cell paste, obtained by lyophilization, was typically 24% of wet cell weight. Acidovorax facilis 72W (ATCC 55746) cells were heated to 50° C. for 1 h in 0.35 M phosphate buffer (pH 7.0) to inactivate nitrile hydratase activity before use as a catalyst.

[0065] Two mutants of the Acidovorax facilis 72W (ATCC 55746) strain have been prepared (U.S. Pat. No. 5,858,736, incorporated by reference) which produce only very low levels of the nitrile hydratase activity of the parent strain. These nitrile hydratase-deficient mutant strains derived from A. facilis 72W (Acidovorax facilis 72-PF-15 (ATCC 55747) and Acidovorax facilis 72-PF-17 (ATCC 55745)), do not require heat-treatment of the cells prior to use as an enzyme catalyst for the hydrolysis of (E,Z)-2M2BN to a mixture of (E)-2M2BA and (Z)-2M2BN.

[0066] Preparation of Cell Extract and Purification of Nitrilase Protein

[0067] All steps in this procedure were performed at 5° C. and at pH 7.5 unless otherwise stated.

[0068] A 25 wt % suspension of Acidovorax facilis 72W (ATCC 55746) wet cell paste was prepared in 20 mM Tris buffer, pH 7.5, 0.1 mM phenylmethylsulfonyl fluoride (PMSF), and 2.0 mM dithiothreitol.

[0069] An extract of this suspension was prepared by passage through a French press (American Instrument Co., Silver Springs, Md., USA) according to methods known to the art. Following a centrifugation at 27,500×g for 30 min to remove cell debris, a 20-55% ammonium sulfate fractionation of the extract was prepared and then concentrated by overnight precipitation following the addition of solid ammonium sulfate to 65% of saturation. The concentrated protein precipitate was reconstituted using a minimum volume of 20 mM Tris, pH 7.5 (Buffer A) and desalted over a PD10 column containing Sephadex G-25 resin (Pharmacia, Milwaukee, Wis.). Following desalting, the concentrated protein extract was fractionated by anion exchange chromatography using a column containing 50 mL of Q-Sparse fast flow (Pharmacia). After loading the column with the concentrated protein extract, the column was washed with three column volumes of Buffer A at a flow rate of 2 mL/min to remove un-adsorbed protein. Adsorbed protein was eluted from the column using a 0-0.5 M NaCl gradient prepared in Buffer A. Elution of protein from the column was monitored at 280 nm.

[0070] Nitrilase activity was monitored throughout purification using an assay measuring the hydrolysis of benzonitrile to produce benzoic acid (Gavagan et al., Appl. Microbiol. Biotechnol., 52:654-659 (1999)). Nitrilase activity eluted at 0.4 M NaCl. Protein components in the 0.4 M NaCl protein fraction were separated by gel electrophoresis (SDS-PAGE) performed under reducing conditions (5% P-mercaptoethanol) on a 10-15% SDS polyacrylamide gel. Greater than 50% of the 0.4 M NaCl protein fraction consisted of a protein with subunit molecular weight of 39.7 kd. Using methods known in the art, the native molecular weight of the nitrilase was determined to be 570 kd following gel filtration chromatography in 20 mM phosphate buffer at pH 7 using a Hiload 16/60 Superdex 200 column (Pharmacia) that had been calibrated using gel filtration MW standards (Pharmacia # 17-0442-01). Following gel filtration, athe nitrilase protein was >90% pure. The specific activity of the purified enzyme was determined to be 35 lU/mg protein using 2-methylglutaronitrile as substrate at 25° C.

[0071] Preparation of Escherichia coli SS1001 (ATCC PTA-1177) and Escherichia coli SW91 (ATCC PTA-1175)

[0072] The nitrilase gene (SEQ ID NO 1) of Acidovorax facilis 72W was cloned and sequenced, and over-expressed in Escherichia colito produce two E. coli transformants, E coli SS1001 (ATCC PTA-1177) and E. coli SW91 (ATCC PTA-1175). These procedures have been described in WO 0175077 A2 (equivalent to U.S. patent application 2001/823373, which is incorporated by reference).

[0073] The nucleotide sequence (SEQ ID NO:3) and deduced amino acid sequence (SEQ ID NO:4) for the nitrilase expressed in E. coli SS1001 contains two minor nucleotide substitutions in comparison to wild type Acidovorax facilis 72W nitrilase sequence. First, the start codon is ATG instead of GTG to facilitate expression in E. Coli. Second, a single nucleotide substitution at position 1098 was introduced during the cloning process, resulting in a corresponding amino acid change of proline (CCA) to serine (TCA) near the C-terminal end of the polypeptide (SEQ ID NOs:3 and 4).

[0074] Growth of Comamonas testosteroni 5-MGAM-4D (ATCC 55744) Comamonas testosteroni 5-MGAM-4D (ATCC 55744) was enriched from soil collected in Orange, Tex., U.S.A., using standard enrichment procedures with E2 basal medium listed below (pH 7.2). E2 Basal Medium g/L KH₂PO₄ 1.4 NaMoO₄.2H₂O 0.0025 NaH₂PO₄ 6.9 NiCl₂.6H₂O 0.01 KCl 0.5 CuSO₄.2H₂O 0.005 MgSO4₄.7H₂O 0.5 Biotin 0.0002 CaCl₂ 0.025 folic acid 0.0002 NaCl 1 pyridoxine.HCl 0.001 sodium citrate 0.1 Riboflavin 0.0005 FeSO₄.7H₂O 0.05 nicotinic acid 0.0005 CoCl₂.6H₂O 0.01 Pantothenic acid 0.0005 MnCl₂.4H₂O 0.001 Vitamin B12 0.00001 ZnCl₂ 0.0005 p-aminobenzoic acid 0.0005 H₃BO₃ 0.000062

[0075] The table below contains modifications that were made to the E2 basal medium for the enrichment described above. Frozen 15% glycerol stocks were maintained at −65° C. to −70° C. Strain Enrichment Nitrile Other Comamonas testosteroni 0.2% 2-methylglutaramide pH 5.6 5-MGAM-4D

[0076]Comamonas testosteroni 5-MGAM-4D was grown aerobically under the following conditions for testing nitrile transformation activity. Strain Nitrile/Amide Medium ° C. Time (h) 5-MGAM-4D 0.2% (w/v) E2, 0.6% (w/v) 30 29 propionamide glucose + Na₂succinate.2H₂O

[0077] Harvested cells were frozen at −65 to −70° C. until used for nitrile transformation.

[0078] Isolation, Growth, and Nitrile Hydrolysis Activity of Comamonas testosteroni S2B-1 (ATCC PTA-5135) and Comamonas testosteroni S5C (ATCC PTA-5134)

[0079]Comamonas testosteroni S2B-1 and Comamonas testosteroni S5C were isolated from extracts of soil collected in Orange, Tex., U.S.A., using standard enrichment procedures using S12-N medium. S12-N medium contains the following: Na₂SO₄, 10 mM; potassium phosphate buffer, pH 7.0, 50 mM; MgCl₂, 2 mM; CaCl₂, 0.7 mM; MnCl₂, 50 μM; FeCl₃, 1 μM; ZnCl₃, 1 μM; CuSO₄, 1.72 μM; CoCl₂, 2.53 μM; Na₂MoO2, 2.42 μM; FeSO₄, 0.0001%; yeast extract, 0.001%; and thiamine hydrochloride, 2 μM. The enrichment culture was established by inoculating 10 μL of soil extract into 10 mL of S12-N medium in a 50 mL Erlenmeyer flask. The enrichment culture was supplemented with 100 ppm 3-hydroxyvaleronitrile (3-HVN) added directly to the culture medium and was incubated at 30° C. with reciprocal shaking. The enrichment culture was maintained by adding 100 ppm of 3-HVN every 2-3 days. The culture was diluted every 4-6 d by replacing 9 mL of the culture with the same volume of S12-N medium. Bacteria that utilize 3-HVN as a sole source of carbon, nitrogen, and energy or as a nitrogen source were isolated by spreading samples of the enrichment culture onto S12-N agar (S12-N medium with 1.5% Difco Noble Agar). 3-HVN (10 PL) was placed on the interior of each Petri dish lid. The Petri dishes were sealed with parafilm and incubated upside down at 28° C. Representative bacterial colonies were then single colony passaged several times on S12-N agar with 3-HVN supplied on the interior of each Petri dish lid. Comamonas testosteroni S2B-1 and Comamonas testosteroni S5C were among the strains isolated using this procedure.

[0080]Comamonas testosteroni S5C was grown in shake flask culture using E2 medium w/3-HVN as sole carbon and nitrogen source. The culture was incubated at 30° C. for 20 h with agitation set to 200 rpm.

[0081]Comamonas testosteroni S2B-1 was grown aerobically for 29 h in al0 L fermentation. An inoculum was prepared by growth of a stock culture of either strain at 32° C. for 15 h in a 2.0 L unbaffled shake flask containing 500 mL of the medium described below in an incubator shaker set at an agitation rate of 300 rpm. At inoculation, the fermentor contained 8.5 L of Fermentor Medium. Dissolved oxygen was held at 25% of saturation, at 32° C., and pH at 6.8-7.0. Fermentor Medium Stock Stock Concen- Concen- Component tration Component tration Fermentor Medium: Potassium phosphate, 1.8 g/L ammonium sulfate, 4.5 g/L monobasic magnesium sulfate, 0.9 g/L Red Star yeast extract 5.0 g/L heptahydrate DL-lactic acid, sodium 15.0 g/L Trace metals (100×) 18 mL/L salt Mazu DF204 antifoam 1.0 mL/L (100× Trace Metal Solution: concentrate) hydrochloric acid 4-5 mL/L zinc sulfate 0.039 g/L calcium chloride, 1.5 g/L heptahydrate dihydrate sodium molybdate 0.3 g/L copper sulfate, 0.38 g/L nickel chloride, 0.25 g/L pentahydrate pentahydrate cobalt chloride, 0.2 g/L ferrous sulfate, 5.0 g/L hexahydrate heptahydrate sodium citrate 10.0 g/L manganese chloride, 0.3 g/L tetrahydrate

[0082] Harvested cells were frozen at −65 to −70° C. until used for nitrile transformation. The 10 L fermentation method described above was also used for the growth of Comamonas testosteroni 5-MGAM-4D. Whole cells of Comamonas testosteroni 5-MGAM-4D, Comamonas testosteroni S2B-1, and Comamonas testosteroni S5C, respectively, were tested for nitrile hydratase and amidase activity using either 3-hydroxyvaleronitrile or 3-hydroxyvaleramide as substrate at a concentration of 0.5 M. A 50 mg (dry cell weight)1 mL cell suspension was prepared in 0.10 M potassium phosphate buffer, pH 7.0. Into a 20-mL glass scintillation vial equipped with a magnetic stir bar was added 3.0 mL of an aqueous solution of either 0.667 M 3-HVA or 0.667 3-HVAm at 25° C. With stirring, 1.0 mL of the cell suspension at 25° C. was added. At 5, 10, and 15 min after the addition of the cell suspension, a 100 μL aliquot was removed from the reaction mixture, mixed with 20 μL of 6.0 N HCl, 100 μL of deionized water, and 200 μL of 0.20 M sodium butyrate (HPLC external standard). Following centrifugation, the supernatant was analyzed by HPLC for the rate of production of either 3-HVAm from 3-HVA or 3-HVA from 3-HVAm.

[0083] A unit of nitrile hydratase or amidase activity (IU) is equivalent to production of 1 micromole 3-HVAm or 3-HVA/min, respectively. The activity level is reported as units per gram of dry cell weight and is reported in the following table (Table 1). TABLE 1 Nitrile Hydratase/Amidase Activity of Comamonas testosteroni S2B-1, Comamonas testosteroni S5C, and Comamonas testosteroni 5-MGAM-4D C. testosteroni Enzyme Activity (U/g dcw) Strain Nitrile Hydratase Amidase S5C 2367  767 S2B-1 4719  976 5-MGAM-4D 7868 1360

[0084] Use of Nitrilase or Nitrile Hydratase/Amidase Biocatalysts for the Regioselective Hydrolysis of (E)-2-Methyl-2-butenenitrile to (E)-2-Methyl-2-butenoic Acid In a Mixture of (E,Z)-2-Methyl-2-butenenitriles

[0085] Intact microbial cells having nitrilase or nitrile hydratase/amidase activities can be used as catalyst without any pretreatment, or the microbial cells may be permeabilized by methods familiar to those skilled in the art, e.g., treatment with toluene, detergents, or freeze thawing, to improve the rate of diffusion of materials into and out of the cells (H. Felix, Anal. Biochem., 120:211-234 (1982)).

[0086] The microbial cell catalyst can be immobilized in a polymer matrix, including but not limited to alginate, carrageenan, polyvinyl alcohol, or polyacrylamide gel, or on a soluble or insoluble support, including but not limited to celite, ion exchange resins, and polymethylmethacrylate, to facilitate recovery and reuse of the catalyst. The enzyme activity or activities can also be isolated from the microbial cells and used directly as catalyst, or the enzyme activity or activities can be immobilized in a polymer matrix or on a soluble or insoluble support. Methods to immobilize cells in a polymer matrix or on a soluble or insoluble support have been widely reported, as have methods for the immobilization of partially-purified or purified enzymes, and are well known to those skilled in the art (see, for example, Methods in Biotechnology, Vol. 1: Immobilization of Enzymes and Cells; Gordon F. Bickerstaff, Editor; Humana Press, Totowa, N.J., USA; 1997).

[0087] Examples of specific enzymes useful in the present invention include, but are not limited to, the Acidovorax facilis 72W nitrilase (ATCC 55746; SEQ ID NOs:1 and 2) and transformants, such as Escherichia coli SS1001, expressing a modified version of the 72W nitrilase (SEQ ID NOs: 3 and 4). Additionally, a combination of nitrile hydratase and amidase activity is also useful in the present invention.

[0088] The concentration of enzyme catalyst in the reaction mixture depends on the catalyst's specific activity and is chosen to obtain the desired rate of reaction. When using unimmobilized intact or permeabilized microbial cells as enzyme catalyst, the wet cell weight (wcw) of the microbial cell catalyst in a reaction mixture typically ranges from 0.001 g to 0.200 g of wet cells per mL of total reaction volume, preferably from 0.002 g to 0.050 g of wet cells per mL. When using immobilized intact or permeabilized microbial cells as enzyme catalyst, the amount of the immobilized cell catalyst in a reaction mixture typically ranges from 0.001 g to 0.400 g of catalyst per mL of total reaction volume, preferably from 0.050 g to 0.250 g of immobilized cell catalyst per mL. Soluble or immobilized enzymes are employed as enzyme catalysts in amounts which vary with the specific activity of the enzyme catalyst, but are typically in the ranges of 0.001 g to 0.050 g of soluble enzyme per mL of total reaction volume, and 0.010 g to 0.200 g of immobilized enzyme per mL of total reaction volume (but not limited to these ranges). The specific activity of a nitrilase catalyst (lU/gram catalyst) is determined by measuring the rate of hydrolysis of (E)-2-methyl-2-butenenitrile to the corresponding carboxylic acid, and the specific activity of a nitrile hydratase/amidase catalyst is determined by measuring the rate of hydration of (E)-2-methyl-2-butenenitrile to the corresponding amide (for nitrile hydratase specific activity) and the rate of hydrolysis of (E)-2-methyl-2-butenamide to the corresponding carboxylic acid (for amidase specific activity) of a 0.14 M solution of the appropriate substrate at 25° C., using a known weight of the catalyst. An IU of enzyme activity is defined as the amount of enzyme activity required to convert one micromole of substrate to product per minute.

[0089] The method of the present invention is useful for converting (E)-2-methyl-2-butenenitrile to the corresponding carboxylic acid. The method of the present invention is also useful for converting (E)-2-methyl-2-butenenitrile in a mixture of (E,Z)-2-methyl-2-butenenitrile to the corresponding carboxylic acid, thereby allowing for the facile recovery of the carboxylic acid (as the ammonium salt) from the product mixture which additionally contains unreacted (Z)-2-methyl-2-butenenitrile (when a nitrilase catalyst is used) or unreacted (Z)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenamide (when a nitrile hydratase/amidase catalyst is used).

[0090] For the biocatalytic conversion of (E)-2-methyl-2-butenenitrile to the corresponding carboxylic acid, an aqueous reaction mixture containing the nitrile is prepared by mixing (E)-2-methyl-2-butenenitrile, or (E,Z)-2-methyl-2-butenenitrile, with an aqueous suspension of the enzyme catalyst. (E)-2-Methyl-2-butenenitrile, (Z)-2-methyl-2-butenenitrile and (E,Z)-2-methyl-2-butenenitrile are only moderately water soluble, ca 1.1 wt % (0.14 M) in the reaction mixture at 22° C. Their solubility also depends on the temperature of the solution and the salt concentration in the aqueous phase; the optional inclusion of a buffer, or the production of the ammonium salt of a carboxylic acid are two possible sources of salt in a reaction mixture.

[0091] In the present application, producing a reaction product at a concentration greater than the solubility limit of the starting nitrile is accomplished using a reaction mixture that is initially composed of two phases: an aqueous phase (containing the enzyme catalyst and dissolved aliphatic or aromatic nitrile) and an organic phase (the undissolved nitrile, optionally dissolved in an organic solvent not miscible with the aqueous phase). As the reaction progresses, the nitrile dissolves into the aqueous phase, eventually yielding a product mixture which may be a single phase, depending on the solubility of the products (and remaining starting material, if any) in water, and on the presence or absence of an optional organic solvent not miscible with water. Examples of optional organic solvents added to a reaction mixture include, but are not limited to, toluene, methyl-t-butyl ether, dichloromethane, and methyl isobutyl ketone.

[0092] The amount of water present in the reaction mixture containing (E)-2-methyl-2-butenenitrile or (E,Z)-2-methyl-2-butenenitrile and an enzyme catalyst may be, at a minimum, only as much water as is sufficient to result in a) complete conversion of the nitrile to the corresponding carboxylic acid, and b) maintenance of the hydrolytic activity of the enzyme catalyst. The reaction may also be run by adding (E)-2-methyl-2-butenenitrile or (E,Z)-2-methyl-2-butenenitrile to the reaction mixture at a rate approximately equal to the enzymatic reaction rate, thereby maintaining a single-phase aqueous reaction mixture, thereby avoiding the potential problem of substrate inhibition of the enzyme at high starting material concentrations.

[0093] The concentration of carboxylic acid product in the reaction mixture (as the ammonium salt) may range from 1 mM to 7 M, preferably between 100 mM and 4 M, and most preferably between 1 M and 3 M. The (E)-2-methyl-2-butenenitrile or (E,Z)-2-methyl-2-butenenitrile may be added to a suitable reaction mixture in one portion, or may be added continuously as the nitrile is hydrolyzed to maintain a low concentration of the nitrile over the course of the reaction, thus limiting any potential inhibitory affects of the starting material or products on the enzyme catalyst activity.

[0094] The temperature of the reaction is chosen to optimize both the reaction rate and the stability of the enzyme catalyst activity. The temperature of the reaction may range from just above the freezing point of the reaction mixture (ca. 0° C.) to 70° C., with a preferred range of reaction temperature of from 5° C. to 45° C. Reactions using the enzyme catalyst may be run unbuffered in water, or in an aqueous reaction mixture containing a buffer (e.g., sodium or potassium phosphate), where the initial pH of the reaction is between 5.0 and 10.0, and preferably between 6.0 and 8.0. As the reaction proceeds, the pH of the reaction mixture may change due to the formation of an ammonium salt of (E)-2-methyl-2-butenoic acid by the hydrolysis of the nitrile functionality of (E)-2-methyl-2-butenenitrile. The reaction can be run to complete conversion of (E)-2-methyl-2-butenenitrile with no pH control, or in the presence of added buffer to control pH, or a suitable acid or base can be added over the course of the reaction to maintain the desired pH.

[0095] The (E)-2-methyl-2-butenoic acid obtained by reaction of a mixture of (E,Z)-2-methyl-2-butenenitrile with a nitrilase catalyst may be readily isolated by first separating any insoluble solid matter (including the enzyme catalyst) from the reaction mixture. (Z)-2-methyl-2-butenenitrile present in the resulting product mixture as a separate organic phase (if any) is separated from the aqueous phase containing (E)-2-methyl-2-butenoic acid (as the ammonium salt) and soluble (Z)-2-methyl-2-butenenitrile. The (Z)-2-methyl-2-butenenitrile present in the aqueous phase is then extracted with a suitable solvent selected from the group consisting of (but not limited to) toluene, heptane, methyl isobutyl ketone, dichloromethane or methyl-t-butyl ether; the ammonium salt of (E)-2-methyl-2-butenoic acid has negligible solubility in the chosen extraction solvent. The (E)-2-methyl-2-butenoic acid product is then isolated from the aqueous phase by procedures well known to those of ordinary skill. Such procedures include but are not limited to concentration, ion exchange, distillation, electrodialysis, extraction, and crystallization. The product may be isolated as the ammonium salt or (after acidification) as the corresponding carboxylic acid. The recovered (Z)-2-methyl-2-butenenitrile, free from any significant concentration of (E)-2-methyl-2-butenenitrile, is then converted to (Z)-2-methyl-2-butenoic acid by procedures well known to those skilled in the art, including those methods for the conversion of nitrites to carboxylic acids disclosed in the present application.

[0096] Similarly, the (E)-2-methyl-2-butenoic acid obtained by reaction of a mixture of (E,Z)-2-methyl-2-butenenitrile with a nitrile hydratase/amidase catalyst may be readily isolated by first separating any insoluble solid matter (including the enzyme catalyst) from the reaction mixture. (Z)-2-methyl-2-butenenitrile (present in the resulting product mixture as a separate organic phase, if any) is separated from the aqueous phase containing (E)-2-methyl-2-butenoic acid (as the ammonium salt), (Z)-2-methyl-2-butenamide (to the extent there is conversion of (Z)-2-methyl-2-butenenitrile, see the accompanying examples) and soluble (Z)-2-methyl-2-butenenitrile. The (Z)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenamide present in the aqueous phase are then extracted with a suitable solvent selected from the group consisting of (but not limited to) toluene, heptane, methyl isobutyl ketone, dichloromethane or methyl-t-butyl ether; the ammonium salt of (E)-2-methyl-2-butenoic acid has negligible solubility in the chosen extraction solvent. The (E)-2-methyl-2-butenoic acid product is then isolated from the aqueous phase by procedures well known to those of ordinary skill. Such procedures include but are not limited to concentration, ion exchange, distillation, electrodialysis, extraction, and crystallization. The product may be isolated as the ammonium salt or (after acidification) as the corresponding carboxylic acid. The recovered (Z)-2-methyl-2-butenenitrile, and (Z)-2-methyl-2-butenamide (if any), free from any significant concentration of (E)-2-methyl-2-butenenitrile, is then converted to (Z)-2-methyl-2-butenoic acid by procedures well known to those skilled in the art, including those methods for the conversion of nitriles or amides to carboxylic acids disclosed in the present application.

EXAMPLES

[0097] The present invention is further defined in the following Examples. It should be understood that these Examples, while indicating preferred embodiments of the invention, are given by way of illustration only. From the above discussion and these Examples, one skilled in the art can ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.

[0098] In the following Examples, the percent recovery of nitrile, and the percent yields of the corresponding amide and carboxylic acid products were based on the initial concentration of nitrile present in the reaction mixture, and were determined by HPLC using a refractive index detector. Analyses for carboxylic acids, amides, and nitrites described in the following examples were performed using a Supelco LC-18-DB column (15 cm×4.6 mm dia.) with precolumn at 25° C. and 10 mM acetic acid, 10 mM sodium acetate in 7.5% methanol in water as eluent at 1.5 mL/min.

Example 1 Hydrolysis of (E)-2-Methyl-2-Butenenitrile to (E)-2-Methyl-2-Butenoic Acid by E. coli SS1001 Cells

[0099] A 5.0 mL suspension of 0.500 g (wet cell paste) E. coli SS1001 cells (ATCC PTA-1177) in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture of 4.91 mL of 50 mM potassium phosphate buffer (pH 7.0) and 80.2 mg of (E)-2-methyl-2-butenenitrile (98.8 mM final concentration of (E)-2-methyl-2-butenenitrile), and the resulting suspension stirred at 35° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)-2-methyl-2-butenenitrile and (E)-2-methyl-2-butenoic acid. After 2.5 h, the conversion of (E)-2-methyl-2-butenenitrile was 100%, and the yield of (E)-2-methyl-2-butenoic acid was 98%; no (E)-2-methyl-2-butenamide was produced over the course of the reaction.

Example 2 Attempted Hydrolysis of (Z)-2-Methyl-2-Butenenitrile to (Z)-2-Methyl-2-Butenoic Acid by E. coli SS1001 Cells (Comparative)

[0100] The procedure described in Example 1 was repeated, except that 79.2 mg of (Z)-2-methyl-2-butenenitrile (97.6 mM final concentration of (Z)-2-methyl-2-butenenitrile) was substituted for (E)-2-methyl-2-butenenitrile. After 3.0 h, the recovery of (Z)-2-methyl-2-butenenitrile was 100%, and there was no conversion to (Z)-2-methyl-2-butenoic acid (0% yield).

Example 3 Reaction of a 1:1 Mixture of (E)- and (Z)-2-Methyl-2-Butenenitrile with E. coli SS001 Cells

[0101] A 5.0 mL suspension of 0.500 g (wet cell paste) E. coli SS1001 cells (ATCC PTA-1177) in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture containing 4.91 mL of 50 mM potassium phosphate buffer (pH 7.0), 38.4 mg of (E)-2-methyl-2-butenenitrile (47.4 mM final concentration of (E)-2-methyl-2-butenenitrile), and 37.7 mg of (Z)-2-methyl-2-butenenitrile (46.5 mM final concentration of (Z)-2-methyl-2-butenenitrile), and the resulting suspension stirred at 25° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)- and (Z)-2-methyl-2-butenenitrile and (E)- and (Z)-2-methyl-2-butenoic acid. After 23 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 100% and 0%, respectively.

Example4 Reaction of a 1:1 Mixture of (E)- and (Z)-2-Methyl-2-Butenenitrile with E. coli SS1001 Cells

[0102] A 5.0 mL suspension of 0.500 g (wet cell paste) E. coli SS1001 cells (ATCC PTA-1177) in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture containing 4.80 mL of 50 mM potassium phosphate buffer (pH 7.0), 80.5 mg of (E)-2-methyl-2-butenenitrile (100 mM final concentration of (E)-2-methyl-2-butenenitrile), and 80.7 mg of (Z)-2-methyl-2-butenenitrile (100 mM final concentration of (Z)-2-methyl-2-butenenitrile), and the resulting suspension stirred at 35° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)- and (Z)-2-methyl-2-butenenitrile and (E)- and (Z)-2-methyl-2-butenoic acid. After 6 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 99% and 0%, respectively.

Example 5 Isomerization 2-Methyl-3-Butenenitrile to a Mixture of (E)- and (Z)-2-Methyl-2-Butenenitrile

[0103] A mixture of 50 g of 2-methyl-3-butenenitrile and 5 g of activity I basic alumina was heated with stirring at 85° C. After 18 h, the conversion of 2-methyl-3-butenenitrile to a mixture of (E)- and (Z)-2-methyl-2-butenenitriles was 100%. The mixture was cooled to ambient temperature and filtered to yield 49.1 g (98% isolated yield) of a mixture of (E)-2-methyl-2-butenenitrile (72 mole %) and (Z)-2-methyl-2-butenenitrile (28 mole %).

Example 6 Reaction of a 72:28 Mixture of (E)- and (Z)-2-Methyl-2-Butenenitriles with E. coli SS1001 Cells

[0104] A 5.0 mL suspension of 0.500 g (wet cell paste) E. coli SS1001 cells (ATCC PTA-1177) in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture containing 4.90 mL of 50 mM potassium phosphate buffer (pH 7.0) and 81.8 mg of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile (101 mM final concentration), and the resulting suspension stirred at 25° C. After 6 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 96% and 0%, respectively.

Example 7 Immobilization of E. coli SS1001 Cells in Calcium Alginate

[0105] Into a 250-mL media bottle equipped with magnetic stir bar and containing 59.7 g of distilled, deionized water at 50° C. was slowly added 3.30 g of FMC BioPolymer Protanal®) LF 10/60 alginate with rapid stirring. The mixture was heated to 75-80° C. with rapid stirring until the alginate was completely dissolved, and the resulting solution cooled to 25° C. in a water bath. To the alginate suspension was added 46.76 g of E. coli SS1001 wet cell paste (19% dry cell weight) and 10.24 mL of distilled water with stirring. The cell/alginate mixture was added dropwise by syringe to 640 mL of 0.20 M calcium acetate buffer (pH 7.0) at 25° C. with stirring. After stirring for 2 h, the buffer was decanted from the resulting beads, which were resuspended in 216 mL of 0.20 M calcium acetate buffer (pH 7.0) at 25° C. With stirring, 4.52 g of 25 wt % glutaraldehyde (GA) in water was added and the beads mixed for 1.0 h at 25° C. To the suspension was then added 18.1 g of 12.5% polyethylenimine (PEI) (BASF Lupasol® PR971 L, average molecular weight ca. 750,000) in water, and the beads mixed for an additional 1 h at 25° C. The crosslinked beads were then washed twice with 270 mL of 5 mM calcium acetate buffer (pH 7.0) at 25° C., and stored in an aqueous buffer containing 1.0 M ammonium acetate, 4 mM calcium acetate, and 10 mM ammonium bicarbonate (pH 7.1) at 5° C.

Example 8 Reaction of a 72:28 Mixture of (E)- and (Z)-2-Methyl-2-Butenenitriles (0.4 M) with Alginate-Immobilized E. coli SS1001 Cells

[0106] Into a 50-mL jacketed reaction vessel equipped with an overhead stirrer (temperature-controlled at 35° C. with a recirculating temperature bath) was placed 1.0 g of GA/PEI-crosslinked E. coli SS1001 cell/alginate beads prepared as described in Example 7. To the reaction vessel was added 18.0 mL of distilled, deionized water, 0.2 mL of 0.20 M calcium acetate buffer (pH 7.0, 2.0 mM final calcium ion concentration in reaction mixture) and 0.798 mL (0.651 g) of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile (0.401 M total concentration), and the mixture stirred at 35° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)- and (Z)-2-methyl-2-butenenitrile and (E)- and (Z)-2-methyl-2-butenoic acid. After 18 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 99% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 99% and 0%, respectively.

Example 9 Reaction of a 72:28 Mixture of (E)- and (Z)-2-Methyl-2-Butenenitriles (1.0 M) with Alginate-Immobilized E. coli SS1001 Cells

[0107] Into a 50-mL jacketed reaction vessel equipped with an overhead stirrer (temperature-controlled at 35° C. with a recirculating temperature bath) was placed 2.0 g of GA/PEI-crosslinked E. coli SS1001 cell/alginate beads prepared as described in Example 7. To the reaction vessel was added 15.8 mL of distilled, deionized water, 0.2 mL of 0.20 M calcium acetate buffer (pH 7.0, 2.0 mM final calcium ion concentration in reaction mixture) and 2.00 mL (1.636 g) of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile (1.01 M total concentration), and the mixture stirred at 35° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)- and (Z)-2-methyl-2-butenenitrile and (E)- and (Z)-2-methyl-2-butenoic acid. After 18 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 100% and 0%, respectively.

Example 10 Reaction of a 72:28 Mixture of (E!- and (Z)-2-Methyl-2-Butenenitriles (2.0 M) with Alginate-Immobilized E. coli SS1001 Cells

[0108] Into a 50-mL jacketed reaction vessel equipped with an overhead stirrer (temperature-controlled at 35° C. with a recirculating temperature bath) was placed 4.0 g of GA/PEI-crosslinked E. coli SS1001 cell/alginate beads prepared as described in Example 7. To the reaction vessel was added 11.8 mL of distilled, deionized water, 0.2 mL of 0.20 M calcium acetate buffer (pH 7.0, 2.0 mM final calcium ion concentration in reaction mixture) and 4.01 mL (3.27 g) of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile (2.02 M total concentration), and the mixture stirred at 35° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was centrifuged, and the supernatant analyzed by HPLC for (E)- and (Z)-2-methyl-2-butenenitrile and (E)- and (Z)-2-methyl-2-butenoic acid. After 22 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 100% and 0%, respectively.

Example 11 Catalyst Recycle in Reactions of a 72:28 Mixture of (E)- and (Z)-2-Methyl-2-Butenenitriles (0.4 M) with Alginate-Immobilized E. coli SS1001 Cells

[0109] Into a 50-mL jacketed reaction vessel equipped with an overhead stirrer (temperature-controlled at 35° C. with a recirculating temperature bath) was placed 4.0 g of GA/PEI-crosslinked E. coli SS1001 cell/alginate beads prepared as described in Example 7. To the reaction vessel was added 15.0 mL of distilled, deionized water, 0.2 mL of 0.20 M calcium acetate buffer (pH 7.0, 2.0 mM final calcium ion concentration in reaction mixture) and 0.802 mL (0.656 g) of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile (0.404 M total concentration), and the mixture stirred at 35° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)- and (Z)-2-methyl-2-butenenitrile and (E)- and (Z)-2-methyl-2-butenoic acid. After 20 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 100% and 0%, respectively.

[0110] At the end of the reaction the product mixture was decanted from the catalyst beads, and an additional 15.1 mL of distilled, deionized water, 0.2 mL of 0.20 M calcium acetate buffer (pH 7.0, 2.0 mM final calcium ion concentration in reaction mixture) and 0.809 mL (0.662 g, 0.407 M) of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile was mixed with the immobilized-cell catalyst at 35° C. After 20 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 97% and 0%, respectively. At the completion of the second reaction with catalyst recycle, the final concentration of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenenitrile were 357 mM and 78.9 mM, respectively.

Example 12 Immobilization of A. facilis 72W Cells in Calcium-crosslinked Alginate

[0111] Into a 250-mL media bottle equipped with magnetic stir bar and containing 59.7 g of distilled, deionized water at 50° C. was slowly added 3.30 g of FMC BioPolymer Protanal® LF 10/60 alginate with rapid stirring. The mixture was heated to 75-80° C. with rapid stirring until the alginate was completely dissolved, and the resulting solution cooled to 25° C. in a water bath. To the alginate suspension was added 37.46 g of A. facilis 72W (ATCC 55746) wet cell paste (24% dry cell weight) and 19.54 mL of distilled water with stirring. The cell/alginate mixture was added dropwise by syringe to 640 mL of 0.20 M calcium acetate buffer (pH 7.0) at 25° C. with stirring. After stirring for 2 h, the buffer was decanted from the resulting beads, which were resuspended in 216 mL of 0.20 M calcium acetate buffer (pH 7.0) at 25° C. With stirring, 4.52 g of 25 wt % glutaraldehyde (GA) in water was added and the beads mixed for 1.0 h at 25° C. To the suspension was then added 18.1 g of 12.5 wt % polyethylenimine (PEI) (BASF Lupasol® PR971L, average molecular weight ca. 750,000) in water, and the beads mixed for an additional 1 h at 25° C. The crosslinked beads were then washed twice with 270 mL of 5 mM calcium acetate buffer (pH 7.0) at 25° C., and stored in an aqueous buffer containing 1.0 M ammonium acetate, 4 mM calcium acetate and 10 mM ammonium bicarbonate (pH 7.1) at 5° C.

Example 13 Catalyst Recycle in Reaction of a 72:28 Mixture of (E)- and (Z)-2-Methyl-2-Butenenitriles (0.4 M) with Alginate-Immobilized A. facilis 72W Cells

[0112] Into a 50-mL jacketed reaction vessel equipped with an overhead stirrer (temperature-controlled at 35° C. with a recirculating temperature bath) was placed 4.0 g of GA/PEI-crosslinked A. facilis 72W cell/alginate beads prepared as described in Example 12. To the reaction vessel was added 15.0 mL of distilled, deionized water, 0.2 mL of 0.20 M calcium acetate buffer (pH 7.0, 2.0 mM final calcium ion concentration in reaction mixture) and 0.796 mL (0.651 g) of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile (0.401 M total concentration), and the mixture stirred at 35° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)- and (Z)-2-methyl-2-butenenitrile and (E)- and (Z)-2-methyl-2-butenoic acid. After 18 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 100% and 0%, respectively.

[0113] At the end of the reaction the product mixture was decanted from the catalyst beads, and an additional 15.0 mL of distilled, deionized water, 0.2 mL of 0.20 M calcium acetate buffer (pH 7.0, 2.0 mM final calcium ion concentration in reaction mixture) and 0.802 mL (0.657 g, 0.405 M) of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile was mixed with the immobilized-cell catalyst at 35° C. After 20 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 97% and 0%, respectively. At the completion of the second reaction with catalyst recycle, the final concentration of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenenitrile were 358 mM and 82.7 mM, respectively.

Example 14 Immobilization of E. coli SS11001 Cells in Carrageenan

[0114] Into a 250 mL media bottle equipped with magnetic stir bar and containing 54.6 g of water at 50° C. was slowly added 2.88 g of kappa-carrageenan (FMC RG300) with rapid stirring. The mixture was heated to 75-80° C. with rapid stirring until the carrageenan was completely dissolved, and the resulting solution cooled to 55-56° C. (gelling temperature ca. 52° C.) in a thermostated water bath. A suspension of 18.6 g of E. coli SS1001 wet cell paste (25.7% dry cell wt) in 19.7 g of 0.35 M sodium phosphate buffer (pH 7.3) was heated to 50° C. for 15 min, then added to the carrageenan solution at 55-56° C. with stirring. The cell/carrageenan mixture was immediately added slowly to 383 mL of soybean oil at 50° C. with stirring using an overhead stirrer. After cell/carrageenan droplets of the desired size were produced in the oil by controlling the stirring rate, the temperature of the oil was reduced to 40-42° C. to gel the droplets, and the oil decanted from the resulting beads. The beads were washed with 150 mL of 0.1 M potassium bicarbonate buffer (pH 7.0), then suspended in 182 mL of this same buffer, and 1.9 g of 25 wt % glutaraldehyde in water was added and the beads mixed for 1 h at 25° C. To the mixture was then added 7.6 g of 12.5 wt % polyethylenimine (BASF Lupasol PR971 L, average Mw ca. 750,000) in water, and the beads mixed for 1 h at 25° C. The beads were then washed twice with 0.30 M ammonium bicarbonate (pH 7.0), and stored in this same buffer at 5° C.

Example 15 Catalyst Recycle in Reaction of a 72:28 Mixture of (E)- and (Z)-2-Methyl-2-Butenenitriles (0.4 M) with Carrageenan-Immobilized E. coli SS1001 Cells

[0115] Into a 50-mL jacketed reaction vessel equipped with an overhead stirrer (temperature-controlled at 35° C. with a recirculating temperature bath) was placed 4.0 g of GA/PEI-crosslinked E. coli SS1001 cell/carrageenan beads prepared as described in Example 14. To the reaction vessel was added 15.2 mL of distilled, deionized water and 0.797 mL (0.652 g) of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile (0.401 M total concentration), and the mixture stirred at 35° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)- and (Z)-2-methyl-2-butenenitrile and (E)- and (Z)-2-methyl-2-butenoic acid. After 18 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 96% and 0%, respectively.

[0116] At the end of the reaction the product mixture was decanted from the catalyst beads, and an additional 15.2 mL of distilled, deionized water and 0.802 mL (0.657 g, 0.405 M) of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile was mixed with the immobilized-cell catalyst at 35° C. After 20 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 0%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 96% and 0%, respectively. At the completion of the second reaction with catalyst recycle, the final concentration of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenenitrile were 353 mM and 81.9 mM, respectively.

Example 16 Isomerization of (Z)-2-pentenitrile to a 78:22 Mixture of (Z)- and (E)-2-Pentenitriles

[0117] A mixture of 402.7 g (4.96 mol) of (Z)-2-pentenitrile, 16.0 g (61.1 mMol) of triphenylphosphine, and 8.4 g (61.6 mmol) of zinc chloride (anhydrous) was heated at 70° C. for 22 h. The resulting mixture was cooled to ambient temperature, and the insoluble zinc chloride filtered from the mixture and the mixture vacuum distilled at 82° C. and 130 torr to separate the resulting mixture of (Z)- and (E)-2-pentenitriles from triphenylphosphine and soluble zinc chloride. The resulting distillate was analyzed by gas chromatography, and the ratio of (Z)- and (E)-2-pentenitriles was 78:22 (mole:mole).

Example 17 Reaction of a 78:22 Mixture of (Z)- and (E)-2-Pentenitriles with E. coli SS1001 Cells (Comparative)

[0118] A 5.0 mL suspension of 0.500 g (wet cell paste) E. coli SS1001 cells (ATCC PTA-1177) in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture containing 4.90 mL of 50 mM potassium phosphate buffer (pH 7.0) and 81.8 mg of a 78:22 mixture of (Z)- and (E)-2-pentenitriles (101 mM final concentration), and the resulting suspension stirred at 35° C. After 4 h, the conversions of (Z)-2-pentenitrile and (E)-2-2-pentenitrile were 100% and 100%, respectively, and the yields of (Z)-2-pentenoic acid and (E)-2-pentenenoic acid were 100% and 100%, respectively.

Example 18 Hydrolysis of 2-Methyl-3-Butenenitrile to 2-Methyl-3-Butenoic Acid by E. coli SS1001 Cells

[0119] A 5.0 mL suspension of 0.500 g (wet cell paste) E. coli SS1001 cells (ATCC PTA-1177) in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture of 4.91 mL of 50 mM potassium phosphate buffer (pH 7.0) and 81.8 mg of 2-methyl-3-butenenitrile (101 mM final concentration), and the resulting suspension stirred at 35° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for 2-methyl-3-butenenitrile and 2-methyl-3-butenoic acid. After 1 h, the conversion of 2-methyl-3-butenenitrile was 100%, and 2-methyl-3-butenoic acid was the only product produced over the course of the reaction.

Example 19 Hydrolysis of (E)-2-Methyl-2-Butenenitrile to (E)-2-Methyl-2-Butenoic Acid by C. testosteroni S2B-1 Cells

[0120] A 5.0 mL suspension of 0.500 g (wet cell paste) C. testosteroni S2B-1 cells (ATCC PTA-5135) in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture of 4.91 mL of 50 mM potassium phosphate buffer (pH 7.0) and 82.1 mg of (E)-2-methyl-2-butenenitrile (101 mM final concentration of (E)-2-methyl-2-butenenitrile), and the resulting suspension stirred at 25° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)-2-methyl-2-butenenitrile and (E)-2-methyl-2-butenoic acid. After 1.5 h, the conversion of (E)-2-methyl-2-butenenitrile was 100%, and the yield of (E)-2-methyl-2-butenoic acid was 99%; no (E)-2-methyl-2-butenamide was observed over the course of the reaction.

Example 20 Hydrolysis of (Z)-2-Methyl-2-Butenenitrile to (Z)-2-Methyl-2-Butenoic acid by C. testosteroni S2B-1 Cells (Comparative)

[0121] The procedure described in Example 19 was repeated, except that 80.6 mg of (Z)-2-methyl-2-butenenitrile (99.3 mM final concentration of (Z)-2-methyl-2-butenenitrile) was substituted for (E)-2-methyl-2-butenenitrile, and the reaction contained 10 mg C. testosteroni 52B-1 cells (wet cell wt.)/mL. After 1.5 h, the recovery of (Z)-2-methyl-2-butenenitrile was 92%, and a 8.4% yield of (Z)-2-methyl-2-butenenamide was obtained; there was no conversion to (Z)-2-methyl-2-butenoic acid (0% yield). After 19 h, the recovery of (Z)-2-methyl-2-butenenitrile was 5.6%, and the yields of (Z)-2-methyl-2-butenenamide and (Z)-2-methyl-2-butenoic acid were 88% and 1.9%, respectively. After 47 h, there was 100% conversion of (Z)-2-methyl-2-butenenitrile, and the yields of (Z)-2-methyl-2-butenenamide and (Z)-2-methyl-2-butenoic acid were 91% and 3.7%, respectively

Example 21 Reaction of a 72:28 Mixture of (E)- and (Z)-2-Methyl-2-Butenenitriles with C. testosteroni S2B-1 Cells

[0122] A 5.0 mL suspension of 0.100 g (wet cell paste) C. testosteroni S2B-1 cells in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture containing 4.90 mL of 50 mM potassium phosphate buffer (pH 7.0) and 84.1 mg of a 72:28 mixture of (E)- and (Z)-2-methyl-2-butenenitrile (104 mM final concentration), and the resulting suspension stirred at 25° C. After 21 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 17%, respectively; the yields of (E)-2-methyl-2-butenamide and (Z)-2-methyl-2-butenamide were 0% and 1.2%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 89% and 0%, respectively. After 47 h, the conversions of (E)-2-methyl-2-butenenitrile and (Z)-2-methyl-2-butenenitrile were 100% and 96%, respectively; the yields of (E)-2-methyl-2-butenamide and (Z)-2-methyl-2-butenamide were 0% and 87%, respectively, and the yields of (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid were 100% and 0%, respectively.

Example 22 Hydrolysis of (E)-2-Methyl-2-Butenenitrile to (E)-2-Methyl-2-Butenoic Acid by C. testosteroni S5C Cells

[0123] A 5.0 mL suspension of 0.050 g (wet cell paste) C. testosteroni S5C cells (ATCC PTA-5134) in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture of 4.91 mL of 50 mM potassium phosphate buffer (pH 7.0) and 81.2 mg of (E)-2-methyl-2-butenenitrile (100 mM final concentration of (E)-2-methyl-2-butenenitrile), and the resulting suspension stirred at 25° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)-2-methyl-2-butenenitrile and (E)-2-methyl-2-butenoic acid. After 2.5 h, the conversion of (E)-2-methyl-2-butenenitrile was 100%, and the yield of (E)-2-methyl-2-butenoic acid was 99%; no (E)-2-methyl-2-butenamide was observed over the course of the reaction.

Example 23 Hydrolysis of (Z)-2-Methyl-2-Butenenitrile to (Z)-2-Methyl-2-Butenoic Acid by C. testosteroni S5C Cells (Comparative)

[0124] The procedure described in Example 22 was repeated, except that 80.6 mg of (Z)-2-methyl-2-butenenitrile (99.4 mM final concentration of (Z)-2-methyl-2-butenenitrile) was substituted for (E)-2-methyl-2-butenenitrile. After 2.5 h, the recovery of (Z)-2-methyl-2-butenenitrile was 75%, and a 23% yield of (Z)-2-methyl-2-butenenamide was obtained; there was no conversion to (Z)-2-methyl-2-butenoic acid (0% yield). After 19 h, the recovery of (Z)-2-methyl-2-butenenitrile was 0.7%, and the yields of (Z)-2-methyl-2-butenenamide and (Z)-2-methyl-2-butenoic acid were 93% and 0%, respectively. After 47 h, there was 100% conversion of (Z)-2-methyl-2-butenenitrile, and the yields of (Z)-2-methyl-2-butenenamide and (Z)-2-methyl-2-butenoic acid were 91% and 3.9%, respectively.

Example 24 Hydrolysis of (E)-2-Methyl-2-Butenenitrile to (E)-2-Methyl-2-Butenoic Acid by C. testosteroni 5-MGAM-4D Cells

[0125] A 5.0 mL suspension of 0.250 g (wet cell paste) C. testosteroni 5-MGAM-4D cells (ATCC 55744) in 50 mM potassium phosphate buffer (pH 7.0) was added to a mixture of 4.91 mL of 50 mM potassium phosphate buffer (pH 7.0) and 81.6 mg of (E)-2-methyl-2-butenenitrile (101 mM final concentration of (E)-2-methyl-2-butenenitrile), and the resulting suspension stirred at 25° C. Samples (0.100 mL) were mixed with 0.900 mL of 60 mM N-ethylacetamide (HPLC external standard) in 1:1 acetonitrile:methanol, the resulting mixture was mixed, centrifuged, and the supernatant analyzed by HPLC for (E)-2-methyl-2-butenenitrile and (E)-2-methyl-2-butenoic acid. After 15 min, the conversion of (E)-2-methyl-2-butenenitrile was 100%, and the yield of (E)-2-methyl-2-butenoic acid was 100%; no (E)-2-methyl-2-butenamide was observed over the course of the reaction.

Example 25 Hydrolysis of (Z)-2-Methyl-2-Butenenitrile to (Z)-2-Methyl-2-Butenoic Acid by C. testosteroni 5-MGAM-4D Cells (Comparative)

[0126] The procedure described in Example 24 was repeated, except that 80.0 mg of (Z)-2-methyl-2-butenenitrile (98.6 mM final concentration of (Z)-2-methyl-2-butenenitrile) was substituted for (E)-2-methyl-2-butenenitrile. After 30 min, the recovery of (Z)-2-methyl-2-butenenitrile was 53%, and a 47% yield of (Z)-2-methyl-2-butenenamide was obtained; there was no conversion to (Z)-2-methyl-2-butenoic acid (0% yield). After 175 min, the conversion of (Z)-2-methyl-2-butenenitrile was 100%, and the yields of (Z)-2-methyl-2-butenenamide and (Z)-2-methyl-2-butenoic acid were 99% and 1.2%, respectively. After 22.5 h, there was 100% conversion of (Z)-2-methyl-2-butenenitrile, and the yields of (Z)-2-methyl-2-butenenamide and (Z)-2-methyl-2-butenoic acid were 89% and 11%, respectively.

Example 26 Preparation of (E)- and (Z)-2-methyl-2-butenoic acids by Enzymatic Hydrolysis of a 72:28 Mixture of (E)- and (Z)-2-Methyl-2-Butenenitriles

[0127] A product mixture produced according to the method described in Example 10, containing ca. 1.44 M (E)-2-methyl-2-butenoic acid and ca. 0.56 M (Z)-2-methyl-2-butenenitrile, is decanted from the immobilized cell catalyst. The resulting product mixture is comprised of an aqueous layer containing the ammonium salt of (E)-2-methyl-2-butenoic acid and ca. 1.1 wt % (Z)-2-methyl-2-butenenitrile, and a second organic layer which is solely (Z)-2-methyl-2-butenenitrile. The (Z)-2-methyl-2-butenenitrile is separated from the aqueous phase, and the aqueous phase is extracted three times with an equivalent volume of methyl-t-butyl ether to remove the remaining (Z)-2-methyl-2-butenenitrile. The pH of the aqueous phase is then adjusted to 2.0 with concentrated hydrochloric acid, and the (E)-2-methyl-2-butenoic acid extracted from the resulting aqueous mixture with methyl-t-butyl ether. The organic extracts are combined, dried over magnesium sulfate, filtered, and the methyl-t-butyl ether removed from the filtrate by distillation under reduced pressure to give (E)-2-methyl-2-butenoic acid in high yield and purity; the (E)-2-methyl-2-butenoic acid is further purified (if desired) by crystallization from ethyl acetate/hexanes.

[0128] The unreacted (Z)-2-methyl-2-butenenitrile recovered from the product mixture is mixed at 10 wt % with 6.0 N sulfuric acid and heated to 100° C. with stirring until complete conversion of (Z)-2-methyl-2-butenenitrile to (Z)-2-methyl-2-butenoic acid is achieved. The (Z)-2-methyl-2-butenoic acid is extracted from the resulting aqueous mixture with methyl-t-butyl ether. The organic extracts are combined, dried over magnesium sulfate, filtered, and the methyl-t-butyl ether is removed from the filtrate by distillation under reduced pressure to give (Z)-2-methyl-2-butenoic acid in high yield and purity. The (Z)-2-methyl-2-butenoic acid is further purified (if desired) by crystallization from ethyl acetate/hexanes.

1 10 1 1110 DNA Acidovorax facilis 72W CDS (1)..(1110) 1 gtg gtt tcg tat aac agc aag ttc ctc gcg gca acc gtt cag gca gag 48 Val Val Ser Tyr Asn Ser Lys Phe Leu Ala Ala Thr Val Gln Ala Glu 1 5 10 15 ccg gta tgg ctc gac gca gac gca acg atc gac aag tcg atc ggc atc 96 Pro Val Trp Leu Asp Ala Asp Ala Thr Ile Asp Lys Ser Ile Gly Ile 20 25 30 atc gaa gaa gct gcc caa aag ggc gcg agt ctg atc gct ttc ccg gaa 144 Ile Glu Glu Ala Ala Gln Lys Gly Ala Ser Leu Ile Ala Phe Pro Glu 35 40 45 gta ttc att ccg ggc tac ccc tat tgg gcg tgg ctc ggc gac gtg aag 192 Val Phe Ile Pro Gly Tyr Pro Tyr Trp Ala Trp Leu Gly Asp Val Lys 50 55 60 tac agc cta agc ttt act tca cgc tat cac gag aat tcg ttg gag cta 240 Tyr Ser Leu Ser Phe Thr Ser Arg Tyr His Glu Asn Ser Leu Glu Leu 65 70 75 80 ggt gac gac cgt atg cgt cgc ctc cag ctg gcc gcg cgc cgc aac aaa 288 Gly Asp Asp Arg Met Arg Arg Leu Gln Leu Ala Ala Arg Arg Asn Lys 85 90 95 atc gca ctc gtc atg ggc tat tcg gag cgg gaa gcc gga tcg cgc tat 336 Ile Ala Leu Val Met Gly Tyr Ser Glu Arg Glu Ala Gly Ser Arg Tyr 100 105 110 ctg agc cag gtg ttc atc gac gag cgt ggc gag atc gtt gcc aat cgg 384 Leu Ser Gln Val Phe Ile Asp Glu Arg Gly Glu Ile Val Ala Asn Arg 115 120 125 cgc aag ctg aag ccc aca cac gtt gag cgt acg atc tac ggc gaa ggc 432 Arg Lys Leu Lys Pro Thr His Val Glu Arg Thr Ile Tyr Gly Glu Gly 130 135 140 aac gga acc gat ttc ctc acg cac gac ttc gcg ttc gga cgc gtc ggt 480 Asn Gly Thr Asp Phe Leu Thr His Asp Phe Ala Phe Gly Arg Val Gly 145 150 155 160 gga ttg aac tgc tgg gaa cat ttc caa ccg ctc agc aag ttc atg atg 528 Gly Leu Asn Cys Trp Glu His Phe Gln Pro Leu Ser Lys Phe Met Met 165 170 175 tac agc ctc ggt gag cag gtc cac gtt gca tcg tgg ccg gcg atg tcc 576 Tyr Ser Leu Gly Glu Gln Val His Val Ala Ser Trp Pro Ala Met Ser 180 185 190 cct ctt cag ccg gat gtt ttc caa ctg agc atc gaa gcc aac gcg acg 624 Pro Leu Gln Pro Asp Val Phe Gln Leu Ser Ile Glu Ala Asn Ala Thr 195 200 205 gtc acc cgc tcg tac gca atc gaa ggc caa acc ttt gtg ctt tgc tcg 672 Val Thr Arg Ser Tyr Ala Ile Glu Gly Gln Thr Phe Val Leu Cys Ser 210 215 220 acg cag gtg atc gga cct agc gcg atc gaa acg ttc tgc ctc aac gac 720 Thr Gln Val Ile Gly Pro Ser Ala Ile Glu Thr Phe Cys Leu Asn Asp 225 230 235 240 gaa cag cgc gca ctg ttg ccg caa gga tgt ggc tgg gcg cgc att tac 768 Glu Gln Arg Ala Leu Leu Pro Gln Gly Cys Gly Trp Ala Arg Ile Tyr 245 250 255 ggc ccg gat gga agc gag ctt gcg aag cct ctg gcg gaa gat gct gag 816 Gly Pro Asp Gly Ser Glu Leu Ala Lys Pro Leu Ala Glu Asp Ala Glu 260 265 270 ggg atc ttg tac gca gag atc gat ctg gag cag att ctg ctg gcg aag 864 Gly Ile Leu Tyr Ala Glu Ile Asp Leu Glu Gln Ile Leu Leu Ala Lys 275 280 285 gct gga gcc gat ccg gtc ggg cac tat tcg cgg cct gac gtg ctg tcg 912 Ala Gly Ala Asp Pro Val Gly His Tyr Ser Arg Pro Asp Val Leu Ser 290 295 300 gtc cag ttc gac ccg cgc aat cat acg cca gtt cat cgc atc ggc att 960 Val Gln Phe Asp Pro Arg Asn His Thr Pro Val His Arg Ile Gly Ile 305 310 315 320 gac ggt cgc ttg gat gtg aat acc cgc agt cgc gtg gag aat ttc cga 1008 Asp Gly Arg Leu Asp Val Asn Thr Arg Ser Arg Val Glu Asn Phe Arg 325 330 335 ctg cga caa gcg gct gag cag gag cgt cag gca tcc aag cgg ctc gga 1056 Leu Arg Gln Ala Ala Glu Gln Glu Arg Gln Ala Ser Lys Arg Leu Gly 340 345 350 acg aaa ctc ttt gaa caa tcc ctt ctg gct gaa gaa ccg gtc cca gca 1104 Thr Lys Leu Phe Glu Gln Ser Leu Leu Ala Glu Glu Pro Val Pro Ala 355 360 365 aag tag 1110 Lys 2 369 PRT Acidovorax facilis 72W 2 Val Val Ser Tyr Asn Ser Lys Phe Leu Ala Ala Thr Val Gln Ala Glu 1 5 10 15 Pro Val Trp Leu Asp Ala Asp Ala Thr Ile Asp Lys Ser Ile Gly Ile 20 25 30 Ile Glu Glu Ala Ala Gln Lys Gly Ala Ser Leu Ile Ala Phe Pro Glu 35 40 45 Val Phe Ile Pro Gly Tyr Pro Tyr Trp Ala Trp Leu Gly Asp Val Lys 50 55 60 Tyr Ser Leu Ser Phe Thr Ser Arg Tyr His Glu Asn Ser Leu Glu Leu 65 70 75 80 Gly Asp Asp Arg Met Arg Arg Leu Gln Leu Ala Ala Arg Arg Asn Lys 85 90 95 Ile Ala Leu Val Met Gly Tyr Ser Glu Arg Glu Ala Gly Ser Arg Tyr 100 105 110 Leu Ser Gln Val Phe Ile Asp Glu Arg Gly Glu Ile Val Ala Asn Arg 115 120 125 Arg Lys Leu Lys Pro Thr His Val Glu Arg Thr Ile Tyr Gly Glu Gly 130 135 140 Asn Gly Thr Asp Phe Leu Thr His Asp Phe Ala Phe Gly Arg Val Gly 145 150 155 160 Gly Leu Asn Cys Trp Glu His Phe Gln Pro Leu Ser Lys Phe Met Met 165 170 175 Tyr Ser Leu Gly Glu Gln Val His Val Ala Ser Trp Pro Ala Met Ser 180 185 190 Pro Leu Gln Pro Asp Val Phe Gln Leu Ser Ile Glu Ala Asn Ala Thr 195 200 205 Val Thr Arg Ser Tyr Ala Ile Glu Gly Gln Thr Phe Val Leu Cys Ser 210 215 220 Thr Gln Val Ile Gly Pro Ser Ala Ile Glu Thr Phe Cys Leu Asn Asp 225 230 235 240 Glu Gln Arg Ala Leu Leu Pro Gln Gly Cys Gly Trp Ala Arg Ile Tyr 245 250 255 Gly Pro Asp Gly Ser Glu Leu Ala Lys Pro Leu Ala Glu Asp Ala Glu 260 265 270 Gly Ile Leu Tyr Ala Glu Ile Asp Leu Glu Gln Ile Leu Leu Ala Lys 275 280 285 Ala Gly Ala Asp Pro Val Gly His Tyr Ser Arg Pro Asp Val Leu Ser 290 295 300 Val Gln Phe Asp Pro Arg Asn His Thr Pro Val His Arg Ile Gly Ile 305 310 315 320 Asp Gly Arg Leu Asp Val Asn Thr Arg Ser Arg Val Glu Asn Phe Arg 325 330 335 Leu Arg Gln Ala Ala Glu Gln Glu Arg Gln Ala Ser Lys Arg Leu Gly 340 345 350 Thr Lys Leu Phe Glu Gln Ser Leu Leu Ala Glu Glu Pro Val Pro Ala 355 360 365 Lys 3 1110 DNA Acidovorax facilis 72W CDS (1)..(1110) 3 atg gtt tcg tat aac agc aag ttc ctc gcg gca acc gtt cag gca gag 48 Met Val Ser Tyr Asn Ser Lys Phe Leu Ala Ala Thr Val Gln Ala Glu 1 5 10 15 ccg gta tgg ctc gac gca gac gca acg atc gac aag tcg atc ggc atc 96 Pro Val Trp Leu Asp Ala Asp Ala Thr Ile Asp Lys Ser Ile Gly Ile 20 25 30 atc gaa gaa gct gcc caa aag ggc gcg agt ctg atc gct ttc ccg gaa 144 Ile Glu Glu Ala Ala Gln Lys Gly Ala Ser Leu Ile Ala Phe Pro Glu 35 40 45 gta ttc att ccg ggc tac ccc tat tgg gcg tgg ctc ggc gac gtg aag 192 Val Phe Ile Pro Gly Tyr Pro Tyr Trp Ala Trp Leu Gly Asp Val Lys 50 55 60 tac agc cta agc ttt act tca cgc tat cac gag aat tcg ttg gag cta 240 Tyr Ser Leu Ser Phe Thr Ser Arg Tyr His Glu Asn Ser Leu Glu Leu 65 70 75 80 ggt gac gac cgt atg cgt cgc ctc cag ctg gcc gcg cgc cgc aac aaa 288 Gly Asp Asp Arg Met Arg Arg Leu Gln Leu Ala Ala Arg Arg Asn Lys 85 90 95 atc gca ctc gtc atg ggc tat tcg gag cgg gaa gcc gga tcg cgc tat 336 Ile Ala Leu Val Met Gly Tyr Ser Glu Arg Glu Ala Gly Ser Arg Tyr 100 105 110 ctg agc cag gtg ttc atc gac gag cgt ggc gag atc gtt gcc aat cgg 384 Leu Ser Gln Val Phe Ile Asp Glu Arg Gly Glu Ile Val Ala Asn Arg 115 120 125 cgc aag ctg aag ccc aca cac gtt gag cgt acg atc tac ggc gaa ggc 432 Arg Lys Leu Lys Pro Thr His Val Glu Arg Thr Ile Tyr Gly Glu Gly 130 135 140 aac gga acc gat ttc ctc acg cac gac ttc gcg ttc gga cgc gtc ggt 480 Asn Gly Thr Asp Phe Leu Thr His Asp Phe Ala Phe Gly Arg Val Gly 145 150 155 160 gga ttg aac tgc tgg gaa cat ttc caa ccg ctc agc aag ttc atg atg 528 Gly Leu Asn Cys Trp Glu His Phe Gln Pro Leu Ser Lys Phe Met Met 165 170 175 tac agc ctc ggt gag cag gtc cac gtt gca tcg tgg ccg gcg atg tcc 576 Tyr Ser Leu Gly Glu Gln Val His Val Ala Ser Trp Pro Ala Met Ser 180 185 190 cct ctt cag ccg gat gtt ttc caa ctg agc atc gaa gcc aac gcg acg 624 Pro Leu Gln Pro Asp Val Phe Gln Leu Ser Ile Glu Ala Asn Ala Thr 195 200 205 gtc acc cgc tcg tac gca atc gaa ggc caa acc ttt gtg ctt tgc tcg 672 Val Thr Arg Ser Tyr Ala Ile Glu Gly Gln Thr Phe Val Leu Cys Ser 210 215 220 acg cag gtg atc gga cct agc gcg atc gaa acg ttc tgc ctc aac gac 720 Thr Gln Val Ile Gly Pro Ser Ala Ile Glu Thr Phe Cys Leu Asn Asp 225 230 235 240 gaa cag cgc gca ctg ttg ccg caa gga tgt ggc tgg gcg cgc att tac 768 Glu Gln Arg Ala Leu Leu Pro Gln Gly Cys Gly Trp Ala Arg Ile Tyr 245 250 255 ggc ccg gat gga agc gag ctt gcg aag cct ctg gcg gaa gat gct gag 816 Gly Pro Asp Gly Ser Glu Leu Ala Lys Pro Leu Ala Glu Asp Ala Glu 260 265 270 ggg atc ttg tac gca gag atc gat ctg gag cag att ctg ctg gcg aag 864 Gly Ile Leu Tyr Ala Glu Ile Asp Leu Glu Gln Ile Leu Leu Ala Lys 275 280 285 gct gga gcc gat ccg gtc ggg cac tat tcg cgg cct gac gtg ctg tcg 912 Ala Gly Ala Asp Pro Val Gly His Tyr Ser Arg Pro Asp Val Leu Ser 290 295 300 gtc cag ttc gac ccg cgc aat cat acg cca gtt cat cgc atc ggc att 960 Val Gln Phe Asp Pro Arg Asn His Thr Pro Val His Arg Ile Gly Ile 305 310 315 320 gac ggt cgc ttg gat gtg aat acc cgc agt cgc gtg gag aat ttc cga 1008 Asp Gly Arg Leu Asp Val Asn Thr Arg Ser Arg Val Glu Asn Phe Arg 325 330 335 ctg cga caa gcg gct gag cag gag cgt cag gca tcc aag cgg ctc gga 1056 Leu Arg Gln Ala Ala Glu Gln Glu Arg Gln Ala Ser Lys Arg Leu Gly 340 345 350 acg aaa ctc ttt gaa caa tcc ctt ctg gct gaa gaa ccg gtc tca gca 1104 Thr Lys Leu Phe Glu Gln Ser Leu Leu Ala Glu Glu Pro Val Ser Ala 355 360 365 aag tag 1110 Lys 4 369 PRT Acidovorax facilis 72W 4 Met Val Ser Tyr Asn Ser Lys Phe Leu Ala Ala Thr Val Gln Ala Glu 1 5 10 15 Pro Val Trp Leu Asp Ala Asp Ala Thr Ile Asp Lys Ser Ile Gly Ile 20 25 30 Ile Glu Glu Ala Ala Gln Lys Gly Ala Ser Leu Ile Ala Phe Pro Glu 35 40 45 Val Phe Ile Pro Gly Tyr Pro Tyr Trp Ala Trp Leu Gly Asp Val Lys 50 55 60 Tyr Ser Leu Ser Phe Thr Ser Arg Tyr His Glu Asn Ser Leu Glu Leu 65 70 75 80 Gly Asp Asp Arg Met Arg Arg Leu Gln Leu Ala Ala Arg Arg Asn Lys 85 90 95 Ile Ala Leu Val Met Gly Tyr Ser Glu Arg Glu Ala Gly Ser Arg Tyr 100 105 110 Leu Ser Gln Val Phe Ile Asp Glu Arg Gly Glu Ile Val Ala Asn Arg 115 120 125 Arg Lys Leu Lys Pro Thr His Val Glu Arg Thr Ile Tyr Gly Glu Gly 130 135 140 Asn Gly Thr Asp Phe Leu Thr His Asp Phe Ala Phe Gly Arg Val Gly 145 150 155 160 Gly Leu Asn Cys Trp Glu His Phe Gln Pro Leu Ser Lys Phe Met Met 165 170 175 Tyr Ser Leu Gly Glu Gln Val His Val Ala Ser Trp Pro Ala Met Ser 180 185 190 Pro Leu Gln Pro Asp Val Phe Gln Leu Ser Ile Glu Ala Asn Ala Thr 195 200 205 Val Thr Arg Ser Tyr Ala Ile Glu Gly Gln Thr Phe Val Leu Cys Ser 210 215 220 Thr Gln Val Ile Gly Pro Ser Ala Ile Glu Thr Phe Cys Leu Asn Asp 225 230 235 240 Glu Gln Arg Ala Leu Leu Pro Gln Gly Cys Gly Trp Ala Arg Ile Tyr 245 250 255 Gly Pro Asp Gly Ser Glu Leu Ala Lys Pro Leu Ala Glu Asp Ala Glu 260 265 270 Gly Ile Leu Tyr Ala Glu Ile Asp Leu Glu Gln Ile Leu Leu Ala Lys 275 280 285 Ala Gly Ala Asp Pro Val Gly His Tyr Ser Arg Pro Asp Val Leu Ser 290 295 300 Val Gln Phe Asp Pro Arg Asn His Thr Pro Val His Arg Ile Gly Ile 305 310 315 320 Asp Gly Arg Leu Asp Val Asn Thr Arg Ser Arg Val Glu Asn Phe Arg 325 330 335 Leu Arg Gln Ala Ala Glu Gln Glu Arg Gln Ala Ser Lys Arg Leu Gly 340 345 350 Thr Lys Leu Phe Glu Gln Ser Leu Leu Ala Glu Glu Pro Val Ser Ala 355 360 365 Lys 5 633 DNA Comamonas testosteroni 5-MGAM-4D CDS (1)..(633) 5 atg ggg caa tca cac acg cat gac cac cat cac gac ggg tac cag gca 48 Met Gly Gln Ser His Thr His Asp His His His Asp Gly Tyr Gln Ala 1 5 10 15 ccg ccc gaa gac atc gcg ctg cgg gtc aag gcc ttg gag tct ctg ctg 96 Pro Pro Glu Asp Ile Ala Leu Arg Val Lys Ala Leu Glu Ser Leu Leu 20 25 30 atc gag aaa ggt ctt gtc gac cca gcg gcc atg gac ttg gtc gtc caa 144 Ile Glu Lys Gly Leu Val Asp Pro Ala Ala Met Asp Leu Val Val Gln 35 40 45 acg tat gaa cac aag gta ggc ccc cga aac ggc gcc aaa gtc gtg gcc 192 Thr Tyr Glu His Lys Val Gly Pro Arg Asn Gly Ala Lys Val Val Ala 50 55 60 aag gcc tgg gtg gac cct gcc tac aag gcc cgt ctg ctg gca gac ggc 240 Lys Ala Trp Val Asp Pro Ala Tyr Lys Ala Arg Leu Leu Ala Asp Gly 65 70 75 80 act gcc ggc att gcc gag ctg ggc ttc tcc ggg gta cag ggc gag gac 288 Thr Ala Gly Ile Ala Glu Leu Gly Phe Ser Gly Val Gln Gly Glu Asp 85 90 95 atg gtc att ctg gaa aac acc ccc gcc gtc cac aac gtc gtc gtt tgc 336 Met Val Ile Leu Glu Asn Thr Pro Ala Val His Asn Val Val Val Cys 100 105 110 acc ttg tgc tct tgc tac cca tgg ccg acg ctg ggc ttg ccc cct gcc 384 Thr Leu Cys Ser Cys Tyr Pro Trp Pro Thr Leu Gly Leu Pro Pro Ala 115 120 125 tgg tac aag gcc ccg ccc tac cgg tcc cgc atg gtg agc gac ccg cgt 432 Trp Tyr Lys Ala Pro Pro Tyr Arg Ser Arg Met Val Ser Asp Pro Arg 130 135 140 ggg gtt ctc gcg gag ttc ggc ctg gtg atc ccc gcg aag gaa atc cgc 480 Gly Val Leu Ala Glu Phe Gly Leu Val Ile Pro Ala Lys Glu Ile Arg 145 150 155 160 gtc tgg gac acc acg gcc gaa ttg cgc tac atg gtg ctg ccg gaa cgg 528 Val Trp Asp Thr Thr Ala Glu Leu Arg Tyr Met Val Leu Pro Glu Arg 165 170 175 ccc gcg gga act gaa gcc tac agc gaa gaa caa ctg gcc gaa ctc gtt 576 Pro Ala Gly Thr Glu Ala Tyr Ser Glu Glu Gln Leu Ala Glu Leu Val 180 185 190 acc cgc gat tcg atg atc ggc acc ggc ctg ccc atc caa ccc acc cca 624 Thr Arg Asp Ser Met Ile Gly Thr Gly Leu Pro Ile Gln Pro Thr Pro 195 200 205 tct cat taa 633 Ser His 210 6 210 PRT Comamonas testosteroni 5-MGAM-4D 6 Met Gly Gln Ser His Thr His Asp His His His Asp Gly Tyr Gln Ala 1 5 10 15 Pro Pro Glu Asp Ile Ala Leu Arg Val Lys Ala Leu Glu Ser Leu Leu 20 25 30 Ile Glu Lys Gly Leu Val Asp Pro Ala Ala Met Asp Leu Val Val Gln 35 40 45 Thr Tyr Glu His Lys Val Gly Pro Arg Asn Gly Ala Lys Val Val Ala 50 55 60 Lys Ala Trp Val Asp Pro Ala Tyr Lys Ala Arg Leu Leu Ala Asp Gly 65 70 75 80 Thr Ala Gly Ile Ala Glu Leu Gly Phe Ser Gly Val Gln Gly Glu Asp 85 90 95 Met Val Ile Leu Glu Asn Thr Pro Ala Val His Asn Val Val Val Cys 100 105 110 Thr Leu Cys Ser Cys Tyr Pro Trp Pro Thr Leu Gly Leu Pro Pro Ala 115 120 125 Trp Tyr Lys Ala Pro Pro Tyr Arg Ser Arg Met Val Ser Asp Pro Arg 130 135 140 Gly Val Leu Ala Glu Phe Gly Leu Val Ile Pro Ala Lys Glu Ile Arg 145 150 155 160 Val Trp Asp Thr Thr Ala Glu Leu Arg Tyr Met Val Leu Pro Glu Arg 165 170 175 Pro Ala Gly Thr Glu Ala Tyr Ser Glu Glu Gln Leu Ala Glu Leu Val 180 185 190 Thr Arg Asp Ser Met Ile Gly Thr Gly Leu Pro Ile Gln Pro Thr Pro 195 200 205 Ser His 210 7 657 DNA Comamonas testosteroni 5-MGAM-4D CDS (1)..(657) 7 atg aat ggc att cac gat act ggg gga gca cat ggt tat ggg ccg gtt 48 Met Asn Gly Ile His Asp Thr Gly Gly Ala His Gly Tyr Gly Pro Val 1 5 10 15 tac aga gaa ccg aac gaa ccc gtc ttt cgc tac gac tgg gaa aaa acg 96 Tyr Arg Glu Pro Asn Glu Pro Val Phe Arg Tyr Asp Trp Glu Lys Thr 20 25 30 gtc atg tcc ctg ttc ccg gcg ctg ttc gcc aac ggc aac ttc aac ctc 144 Val Met Ser Leu Phe Pro Ala Leu Phe Ala Asn Gly Asn Phe Asn Leu 35 40 45 gat gag ttt cga cac ggc atc gag cgc atg aac ccc atc gac tac ctg 192 Asp Glu Phe Arg His Gly Ile Glu Arg Met Asn Pro Ile Asp Tyr Leu 50 55 60 aag gga acc tac tac gaa cac tgg atc cat tcc atc gaa acc ttg ctg 240 Lys Gly Thr Tyr Tyr Glu His Trp Ile His Ser Ile Glu Thr Leu Leu 65 70 75 80 gtc gaa aag ggt gtg ctc acg gca acg gaa ctc gcg acc ggc aag gca 288 Val Glu Lys Gly Val Leu Thr Ala Thr Glu Leu Ala Thr Gly Lys Ala 85 90 95 tct ggc aag aca gcg aca ccg gtg ctg acg ccg gcc atc gtg gac gga 336 Ser Gly Lys Thr Ala Thr Pro Val Leu Thr Pro Ala Ile Val Asp Gly 100 105 110 ctg ctc agc acc ggg gct tct gcc gcc cgg gag gag ggt gcg cgg gcg 384 Leu Leu Ser Thr Gly Ala Ser Ala Ala Arg Glu Glu Gly Ala Arg Ala 115 120 125 cgg ttc gct gtg ggg gac aag gtt cgc gtc ctc aac aag aac ccg gtg 432 Arg Phe Ala Val Gly Asp Lys Val Arg Val Leu Asn Lys Asn Pro Val 130 135 140 ggc cat acc cgc atg ccg cgc tac acg cgg ggc aaa gtg ggg aca gtg 480 Gly His Thr Arg Met Pro Arg Tyr Thr Arg Gly Lys Val Gly Thr Val 145 150 155 160 gtc atc gac cat ggt gtg ttc gtg acg ccg gac acc gcg gca cac gga 528 Val Ile Asp His Gly Val Phe Val Thr Pro Asp Thr Ala Ala His Gly 165 170 175 aag ggc gag cac ccc cag cac gtt tac acc gtg agt ttc acg tcg gtc 576 Lys Gly Glu His Pro Gln His Val Tyr Thr Val Ser Phe Thr Ser Val 180 185 190 gaa ctg tgg ggg caa gac gcc tcc tcg ccg aag gac acg att cgc gtc 624 Glu Leu Trp Gly Gln Asp Ala Ser Ser Pro Lys Asp Thr Ile Arg Val 195 200 205 gac ttg tgg gat gac tac ctg gag cca gcg tga 657 Asp Leu Trp Asp Asp Tyr Leu Glu Pro Ala 210 215 8 218 PRT Comamonas testosteroni 5-MGAM-4D 8 Met Asn Gly Ile His Asp Thr Gly Gly Ala His Gly Tyr Gly Pro Val 1 5 10 15 Tyr Arg Glu Pro Asn Glu Pro Val Phe Arg Tyr Asp Trp Glu Lys Thr 20 25 30 Val Met Ser Leu Phe Pro Ala Leu Phe Ala Asn Gly Asn Phe Asn Leu 35 40 45 Asp Glu Phe Arg His Gly Ile Glu Arg Met Asn Pro Ile Asp Tyr Leu 50 55 60 Lys Gly Thr Tyr Tyr Glu His Trp Ile His Ser Ile Glu Thr Leu Leu 65 70 75 80 Val Glu Lys Gly Val Leu Thr Ala Thr Glu Leu Ala Thr Gly Lys Ala 85 90 95 Ser Gly Lys Thr Ala Thr Pro Val Leu Thr Pro Ala Ile Val Asp Gly 100 105 110 Leu Leu Ser Thr Gly Ala Ser Ala Ala Arg Glu Glu Gly Ala Arg Ala 115 120 125 Arg Phe Ala Val Gly Asp Lys Val Arg Val Leu Asn Lys Asn Pro Val 130 135 140 Gly His Thr Arg Met Pro Arg Tyr Thr Arg Gly Lys Val Gly Thr Val 145 150 155 160 Val Ile Asp His Gly Val Phe Val Thr Pro Asp Thr Ala Ala His Gly 165 170 175 Lys Gly Glu His Pro Gln His Val Tyr Thr Val Ser Phe Thr Ser Val 180 185 190 Glu Leu Trp Gly Gln Asp Ala Ser Ser Pro Lys Asp Thr Ile Arg Val 195 200 205 Asp Leu Trp Asp Asp Tyr Leu Glu Pro Ala 210 215 9 1407 DNA Comamonas testosteroni 5-MGAM-4D CDS (1)..(1407) 9 atg agt tcg cta acc cgc ctc acc ctc gcg caa gtt gcg cag aaa ctt 48 Met Ser Ser Leu Thr Arg Leu Thr Leu Ala Gln Val Ala Gln Lys Leu 1 5 10 15 aag gca cgg gaa gtc tcc gcc gtt gaa gtt ctg gac gcc tgt ctg acg 96 Lys Ala Arg Glu Val Ser Ala Val Glu Val Leu Asp Ala Cys Leu Thr 20 25 30 cag gtg cgc tcc acc gaa aaa cag atc agt gcg tac gtg tgc gtg ctg 144 Gln Val Arg Ser Thr Glu Lys Gln Ile Ser Ala Tyr Val Cys Val Leu 35 40 45 gag gat cag gcc cgt gca gca gcc cag caa gct gac gcc gac atc agc 192 Glu Asp Gln Ala Arg Ala Ala Ala Gln Gln Ala Asp Ala Asp Ile Ser 50 55 60 gcc ggg cgc tgg aaa ggc ccg ctg cat ggc gtg cct gta gcg gtc aag 240 Ala Gly Arg Trp Lys Gly Pro Leu His Gly Val Pro Val Ala Val Lys 65 70 75 80 gac tta tac gac atc gct ggc gta ccc acc acg gca tcg tcg cgc cag 288 Asp Leu Tyr Asp Ile Ala Gly Val Pro Thr Thr Ala Ser Ser Arg Gln 85 90 95 cgc acg aat tgg acg ccg cag caa gac tgc gcc gta gtc cgg cgc ttg 336 Arg Thr Asn Trp Thr Pro Gln Gln Asp Cys Ala Val Val Arg Arg Leu 100 105 110 aaa gac gca ggt gcc gtt atc ctt ggc aag acc cat acg cac gaa ttc 384 Lys Asp Ala Gly Ala Val Ile Leu Gly Lys Thr His Thr His Glu Phe 115 120 125 gcc tat ggc gtc atc act ccg aag tcg cgc aac ccc tgg gac ccg gga 432 Ala Tyr Gly Val Ile Thr Pro Lys Ser Arg Asn Pro Trp Asp Pro Gly 130 135 140 aga aca ccg ggt ggc tcc agc ggc ggc tcg gcg gcc acg gtc gca gcc 480 Arg Thr Pro Gly Gly Ser Ser Gly Gly Ser Ala Ala Thr Val Ala Ala 145 150 155 160 tgc ggc gtc tac ttg gcg acc ggc acc gac acc ggt gga tcc gtt cgc 528 Cys Gly Val Tyr Leu Ala Thr Gly Thr Asp Thr Gly Gly Ser Val Arg 165 170 175 atc cct tcg tcg atg tgc aac acc gta ggc ctg aag cca acc tac ggg 576 Ile Pro Ser Ser Met Cys Asn Thr Val Gly Leu Lys Pro Thr Tyr Gly 180 185 190 cgc gtg agc cgt gcc ggt gtg agt tca ctt tcc tgg agc ctg gac cat 624 Arg Val Ser Arg Ala Gly Val Ser Ser Leu Ser Trp Ser Leu Asp His 195 200 205 cca ggc ccg atc acg cgc acc gtg gaa gac acg gcg ctc agc ctt cag 672 Pro Gly Pro Ile Thr Arg Thr Val Glu Asp Thr Ala Leu Ser Leu Gln 210 215 220 gtg atg gct ggc ttc gat cca gcc gac cgc ggc tcg ttg gat gag ccg 720 Val Met Ala Gly Phe Asp Pro Ala Asp Arg Gly Ser Leu Asp Glu Pro 225 230 235 240 gtg ccc agc tat gcc gaa ggg ctc ggc caa ggc gtg aaa ggc ctg cgc 768 Val Pro Ser Tyr Ala Glu Gly Leu Gly Gln Gly Val Lys Gly Leu Arg 245 250 255 gtg ggc gtg ccg aag aac tac ttc ttc gac cgc gtg gac ccg gaa gtt 816 Val Gly Val Pro Lys Asn Tyr Phe Phe Asp Arg Val Asp Pro Glu Val 260 265 270 gaa agt gcg gtt cgt gcc gcc atc gat caa ctg aaa gag ctg ggc gcc 864 Glu Ser Ala Val Arg Ala Ala Ile Asp Gln Leu Lys Glu Leu Gly Ala 275 280 285 gaa ctg gtg gaa gtc gaa gtg ccc atg gcc gag cag atc atc ccg gtg 912 Glu Leu Val Glu Val Glu Val Pro Met Ala Glu Gln Ile Ile Pro Val 290 295 300 gag ttc ggg atc gtg cta ccc gaa gcc agc gcc tac cac cgc acg atg 960 Glu Phe Gly Ile Val Leu Pro Glu Ala Ser Ala Tyr His Arg Thr Met 305 310 315 320 ctg cgc gag tca ccc gag ctc tac acc gcc gat gtc cgc ata ctg ctg 1008 Leu Arg Glu Ser Pro Glu Leu Tyr Thr Ala Asp Val Arg Ile Leu Leu 325 330 335 gaa ctc gga aat cta gtc acc gcc acc gac tac ctg cag gcg cag cgc 1056 Glu Leu Gly Asn Leu Val Thr Ala Thr Asp Tyr Leu Gln Ala Gln Arg 340 345 350 gtc cgt acg ctg atg cag cgc gcg gtg gcc gag atg ttc cag cgc atc 1104 Val Arg Thr Leu Met Gln Arg Ala Val Ala Glu Met Phe Gln Arg Ile 355 360 365 gat gtg ctg atc gca ccc aca ctg ccc atc ccg gct gct cgc agc ggg 1152 Asp Val Leu Ile Ala Pro Thr Leu Pro Ile Pro Ala Ala Arg Ser Gly 370 375 380 gag gag gtc cac aca tgg ccg gac ggc acg gta gag gcg ttg ttc atg 1200 Glu Glu Val His Thr Trp Pro Asp Gly Thr Val Glu Ala Leu Phe Met 385 390 395 400 gcc tat acg cgc ttc acc tcg ttc ggc aac gtg aca gga tta ccc acg 1248 Ala Tyr Thr Arg Phe Thr Ser Phe Gly Asn Val Thr Gly Leu Pro Thr 405 410 415 ctg aac ctg ccc tgt ggt ttc tcc aag gat ggg ttg ccg atc ggc atg 1296 Leu Asn Leu Pro Cys Gly Phe Ser Lys Asp Gly Leu Pro Ile Gly Met 420 425 430 cag atc acc ggc cgg ccg ctg gac gag aag acc ctg ctg cgt gct ggg 1344 Gln Ile Thr Gly Arg Pro Leu Asp Glu Lys Thr Leu Leu Arg Ala Gly 435 440 445 ctg gcc tac gag aaa gcc acg acc tgg cac cag cgt cat ccg gaa ctg 1392 Leu Ala Tyr Glu Lys Ala Thr Thr Trp His Gln Arg His Pro Glu Leu 450 455 460 atc gga gcg ggc tga 1407 Ile Gly Ala Gly 465 10 468 PRT Comamonas testosteroni 5-MGAM-4D 10 Met Ser Ser Leu Thr Arg Leu Thr Leu Ala Gln Val Ala Gln Lys Leu 1 5 10 15 Lys Ala Arg Glu Val Ser Ala Val Glu Val Leu Asp Ala Cys Leu Thr 20 25 30 Gln Val Arg Ser Thr Glu Lys Gln Ile Ser Ala Tyr Val Cys Val Leu 35 40 45 Glu Asp Gln Ala Arg Ala Ala Ala Gln Gln Ala Asp Ala Asp Ile Ser 50 55 60 Ala Gly Arg Trp Lys Gly Pro Leu His Gly Val Pro Val Ala Val Lys 65 70 75 80 Asp Leu Tyr Asp Ile Ala Gly Val Pro Thr Thr Ala Ser Ser Arg Gln 85 90 95 Arg Thr Asn Trp Thr Pro Gln Gln Asp Cys Ala Val Val Arg Arg Leu 100 105 110 Lys Asp Ala Gly Ala Val Ile Leu Gly Lys Thr His Thr His Glu Phe 115 120 125 Ala Tyr Gly Val Ile Thr Pro Lys Ser Arg Asn Pro Trp Asp Pro Gly 130 135 140 Arg Thr Pro Gly Gly Ser Ser Gly Gly Ser Ala Ala Thr Val Ala Ala 145 150 155 160 Cys Gly Val Tyr Leu Ala Thr Gly Thr Asp Thr Gly Gly Ser Val Arg 165 170 175 Ile Pro Ser Ser Met Cys Asn Thr Val Gly Leu Lys Pro Thr Tyr Gly 180 185 190 Arg Val Ser Arg Ala Gly Val Ser Ser Leu Ser Trp Ser Leu Asp His 195 200 205 Pro Gly Pro Ile Thr Arg Thr Val Glu Asp Thr Ala Leu Ser Leu Gln 210 215 220 Val Met Ala Gly Phe Asp Pro Ala Asp Arg Gly Ser Leu Asp Glu Pro 225 230 235 240 Val Pro Ser Tyr Ala Glu Gly Leu Gly Gln Gly Val Lys Gly Leu Arg 245 250 255 Val Gly Val Pro Lys Asn Tyr Phe Phe Asp Arg Val Asp Pro Glu Val 260 265 270 Glu Ser Ala Val Arg Ala Ala Ile Asp Gln Leu Lys Glu Leu Gly Ala 275 280 285 Glu Leu Val Glu Val Glu Val Pro Met Ala Glu Gln Ile Ile Pro Val 290 295 300 Glu Phe Gly Ile Val Leu Pro Glu Ala Ser Ala Tyr His Arg Thr Met 305 310 315 320 Leu Arg Glu Ser Pro Glu Leu Tyr Thr Ala Asp Val Arg Ile Leu Leu 325 330 335 Glu Leu Gly Asn Leu Val Thr Ala Thr Asp Tyr Leu Gln Ala Gln Arg 340 345 350 Val Arg Thr Leu Met Gln Arg Ala Val Ala Glu Met Phe Gln Arg Ile 355 360 365 Asp Val Leu Ile Ala Pro Thr Leu Pro Ile Pro Ala Ala Arg Ser Gly 370 375 380 Glu Glu Val His Thr Trp Pro Asp Gly Thr Val Glu Ala Leu Phe Met 385 390 395 400 Ala Tyr Thr Arg Phe Thr Ser Phe Gly Asn Val Thr Gly Leu Pro Thr 405 410 415 Leu Asn Leu Pro Cys Gly Phe Ser Lys Asp Gly Leu Pro Ile Gly Met 420 425 430 Gln Ile Thr Gly Arg Pro Leu Asp Glu Lys Thr Leu Leu Arg Ala Gly 435 440 445 Leu Ala Tyr Glu Lys Ala Thr Thr Trp His Gln Arg His Pro Glu Leu 450 455 460 Ile Gly Ala Gly 465 

What is claimed is:
 1. A process for producing (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid in high yield and purity from a mixture of (E,Z)-2-methyl-2-butenenitriles comprising (a) contacting a mixture of (E,Z)-2-methyl-2-butenenitriles in a suitable aqueous reaction mixture with a catalyst having Acidovorax facilis 72W (ATCC 55746) nitrilase activity; (b) separating the (E)-2-methyl-2-butenoic acid produced in step (a) in the form of a salt or acid from unreacted (Z)-2-methyl-2-butenenitrile; and (c) converting the unreacted (Z)-2-methyl-2-butenenitrile from step (b) to (Z)-2-methyl-2-butenoic acid in the form of a salt or acid.
 2. The process of claim 1 wherein the catalyst is in the form of intact microbial cells, permeabilized microbial cells, one or more cell components of a microbial cell extract, partially-purified enzyme(s), or purified enzyme(s).
 3. The process of claim 2 wherein the catalyst is in the form of microbial cells transformed to express Acidovorax facilis 72W nitrilase.
 4. The process of claim 1 wherein the catalyst is in the form of microbial cells selected from the group consisting of Acidovorax facilis 72-PF-17 (ATCC 55745), Acidovorax facilis 72-PF-15 (ATCC 55747), Escherichia coli SS1001 (ATCC PTA-1177), and Escherichia coli SW91 (ATCC PTA-1175).
 5. The process of claim 2 further comprising before step (a) heating the catalyst Acidovorax facilis 72W (ATCC 55746) to a temperature of about 35° C. to 70° C. for between 10 and 120 minutes, whereby nitrile hydratase activity is inactivated, and nitrilase activity is preserved.
 6. The process of claim 2 wherein the catalyst is immobilized in or on a soluble or insoluble support.
 7. A process for producing (E)-2-methyl-2-butenoic acid and (Z)-2-methyl-2-butenoic acid in high yield and purity from a mixture of (E,Z)-2-methyl-2-butenenitriles comprising (a) contacting a mixture of (E,Z)-2-methyl-2-butenenitriles in a suitable aqueous reaction mixture with a catalyst expressing nitrile hydratase and amidase activities and selected from the group consisting of Comamonas testosteroni 5-MGAM-4D (ATCC 55744), Comamonas testosteroni S2B-1 (ATCC PTA-5135), and Comamonas testosteroni S5C (ATCC PTA-5134); (b) separating the (E)-2-methyl-2-butenoic acid produced in step (a) in the form of a salt or acid from (Z)-2-methyl-2-butenamide and unreacted (Z)-2-methyl-2-butenenitrile; and (c) treating the (Z)-2-methyl-2-butenamide and unreacted (Z)-2-methyl-2-butenenitrile from step (b) with a suitable catalyst or chemical reagent to produce (Z)-2-methyl-2-butenoic acid in the form of a salt or acid.
 8. The process of claim 7 further comprising before step (a) heating the catalyst of Comamonas testosteroni 5-MGAM-4D (ATCC 55744) to a temperature of about 35° C. to 70° C. for between 10 and 120 minutes, whereby nitrile hydratase activity is inactivated, and nitrile hydratase and amidase activities are preserved.
 9. The process of claim 8 wherein the enzyme catalyst is immobilized in or on a soluble or insoluble support.
 10. A process for producing (E)-2-methyl-2-butenoic acid in high yield and purity from (E)-2-methyl-2-butenenitrile comprising (a) contacting (E)-2-methyl-2-butenenitrile in a suitable aqueous reaction mixture with a catalyst expressing Acidovorax facilis 72W (ATCC 55746) nitrilase activity; and (b) isolating (E)-2-methyl-2-butenoic acid from step (b) in the form of a salt or acid.
 11. A process for producing (E)-2-methyl-2-butenoic acid in high yield and purity from (E)-2-methyl-2-butenenitrile comprising (a) contacting (E)-2-methyl-2-butenenitrile in a suitable aqueous reaction mixture with a catalyst expressing nitrile hydratase and amidase activities and selected from the group consisting of Comamonas testosteroni 5-MGAM-4D (ATCC 55744), Comamonas testosteroni S2B-1 (ATCC PTA-5135), and Comamonas testosteroni S5C (ATCC PTA-5134); and (b) isolating (E)-2-methyl-2-butenoic acid from step (b) in the form of a salt or acid.
 12. A purified Comamonas testosteroni strain S2B-1 having regioselective nitrile hydratase and amidase activity and designated ATCC PTA-5135.
 13. A purified Comamonas testosteroni strain S5C having regioselective nitrile hydratase and amidase activity and designated ATCC PTA-5134. 